Neurofibromatosis 1 (NF1) is a common neurocutaneous condition with an autosomal dominant pattern of inheritance. The complications are diverse and disease expression varies, even within families. Progress in molecular biology and neuroimaging and the development of mouse models have helped to elucidate the aetiology of NF1 and its clinical manifestations. Furthermore, these advances have raised the prospect of therapeutic intervention for this complex and distressing disease. Members of the United Kingdom Neurofibromatosis Association Clinical Advisory Board collaborated to produce a consensus statement on the current guidelines for diagnosis and management of NF1. The proposals are based on published clinical studies and on the pooled knowledge of experts in neurofibromatosis with experience of providing multidisciplinary clinical and molecular services for NF1 patients. The consensus statement discusses the diagnostic criteria, major differential diagnoses, clinical manifestations and the present strategies for monitoring and management of NF1 complications.
- MPNST, malignant peripheral nerve sheath tumours
- NF1, NF2, neurofibromatosis 1, 2
- OPG, optic pathway gliomas
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- MPNST, malignant peripheral nerve sheath tumours
- NF1, NF2, neurofibromatosis 1, 2
- OPG, optic pathway gliomas
Descriptions of individuals purported to have neurofibromatosis have been discovered in manuscripts dating from 1000 AD.1 However, it was not until 1881 that von Recklinghausen coined the term “neurofibroma” when he observed that this benign tumour arose from the peripheral nerve sheath.2 His colleagues honoured his contribution by naming the condition von Recklinghausen’s disease. However, the different forms of neurofibromatosis were not separated and delineated until the latter part of the twentieth century (tables 1, 2). The National Institutes of Health Consensus Development Conference formulated the diagnostic criteria for neurofibromatosis 1 (NF1), underlining the pivotal involvement of the skin, bone and the nervous system in the condition (table 1).3 In 1990, the NF1 gene was cloned on chromosome 17q11.2.4,5 Neurofibromin, the gene product, is ubiquitously expressed at high levels in the nervous system and functions as a tumour suppressor.6–8 Loss of neurofibromin through mutation leads to an increased risk of developing benign and malignant tumours in affected individuals.
DIAGNOSIS OF NF1
These diagnostic criteria are robust and have stood the test of time well. Clinicians should be aware that some individuals with mosaic/segmental NF1 fulfil the diagnostic criteria as they present with six or more café au lait patches with skin-fold freckling or neurofibromas. However, the skin manifestations are in a restricted segment of the body (see section on differential diagnosis).10 Approximately half of NF1 sufferers are the first in their family to have the condition.11 Children with six café au lait patches alone and no family history should be followed up as if they have the disease, as 95% of them will develop NF1.12 Occasionally, other signs of NF1 may not develop until late teens or early twenties and slit lamp examination for Lisch nodules might be helpful in these children. NF1 mutational analysis clarifies the diagnosis in some uncertain cases and in individuals contemplating prenatal diagnosis (see section on prenatal diagnosis). However, genetic testing is not advocated routinely and expert consultation is advised before it is undertaken. Furthermore, biopsy of asymptomatic cutaneous neurofibromas should not be undertaken for diagnostic purposes in individuals with clearcut NF1.
Hyperintense lesions on T2 weighted brain MRI (formerly called UBOs) are probably caused by aberrant myelination or gliosis, and are pathognomonic of NF1.13 They occur most commonly in children of 8–16 years old, tend to disappear in adulthood and have a tenuous link with cognitive impairment (see section on cognitive impairment).14–16 The presence of these lesions can assist the diagnosis of NF1 but MRI under anaesthetic is not warranted for this purpose in young children.17
Differential diagnosis of NF1
The differential diagnoses of NF1 include other forms of neurofibromatosis, conditions with café au lait patches or with pigment changes confused with café au lait patches. Likewise, tumours or localised body overgrowth can be mistaken for neurofibromas (table 2).18–24
It should be emphasised that one or two café au lait patches occur in 10% of the general population. Children with 3–5 café au lait patches but no other signs of NF1 should be followed up in a specialist neurofibromatosis clinic as they might have mosaic NF1 or neurofibromatosis 2 (NF2). Mosaic NF1 occurs as a result of a somatic mutation in the NF1 gene, the proportion of the body affected depending on the time of the mutation in embryonic development.10 The importance of making the diagnosis is that NF1 complications are relatively infrequent in segmental NF1 and there is a much lower risk of recurrence in offspring. Homozygotes for one of the genes causing hereditary non-polyposis cancer of the colon have café au lait patches and an affected first degree relative. However, the affected relative is a sibling and the parents are normal.19
The only subtype of NF1 that is distinct and has a uniform phenotype in families is Watson syndrome. It is characterised by pulmonary stenosis, cognitive impairment, café au lait patches and few, if any, cutaneous neurofibromas.18 There is no clear evidence that neurofibromatosis–Noonan syndrome exists as a distinct phenotype with features of both syndromes. It is likely that some individuals with NF1 simply have facial features akin to those of Noonan syndrome and these characteristics are not consistent within families. Molecular studies indicate that neurofibromatosis–Noonan syndrome is caused by mutations of the NF1 gene, some of which have been identified in patients with classical NF1.20
NF2 is an autosomal dominant neurocutaneous disease that is clinically and genetically distinct from NF1 and occurs in approximately 1 in 25 000 individuals.21 It is caused by inactivating mutations on chromosome 22q11.2 and is characterised by bilateral vestibular schwannomas.22,23 Affected individuals also develop schwannomas on other cranial, spinal, peripheral and cutaneous nerves. Café au lait patches are less numerous than in NF1 and the skin lesions are predominantly schwannomas. Central nervous system meningiomas and gliomas are observed and slit lamp examination reveals juvenile subcapsular lens opacities in the majority of patients.23
Subcutaneous, peripheral nerve and spinal schwannomas develop in schwannomatosis without vestibular schwannomas or the ophthalmological features of NF2.24
Multiple lipomas occur primarily on the trunk, proximal thighs and distal arms, and are inherited in an autosomal dominant fashion. Biopsy is sometimes necessary to differentiate cutaneous neurofibromas from schwannomas and lipomas.
ASSESSMENT AND MANAGEMENT OF CLINICAL PROBLEMS
Once the diagnosis is considered, referral should be made to any clinician skilled in the diagnosis of NF1, including geneticists, paediatricians, neurologists or dermatologists. Routine screening investigations are not recommended for the detection of the majority of complications associated with the condition. However, visual assessment should be performed in young children because they do not complain of visual impairment (see section on optic pathway glioma). Furthermore, given the high frequency of learning and behavioural problems in NF1 children, monitoring is essential (see section on cognitive impairment). Baseline brain and spine MRI, and routine imaging of the chest and abdomen to identify asymptomatic tumours, do not influence management and should not be undertaken.
The mainstay of management is age specific monitoring of disease manifestations and patient education. At all ages it is most likely that severe disease complications such as malignant peripheral nerve sheath tumours (MPNST) will become symptomatic between appointments. NF1 individuals need to be encouraged to seek review of any unusual symptoms and ask if they are related to NF1. All children with uncomplicated disease need to be assessed once a year (table 3), ideally by one paediatrician in each area to facilitate coordinated care. Older adults should be offered the opportunity of attending the clinic on an annual basis. Young adults aged 16–25 years are at a vulnerable stage of life and require education about NF1 and its possible complications. Counselling about disease inheritance and psychological support are advised, particularly as neurofibromas often start to develop in late adolescence.
Monitoring after the mid-twenties depends on patient preference and disease severity. Adults with severe disease have usually been identified by this stage and require lifelong monitoring in an NF1 clinic. Adults with mild disease have a much lower risk of complications. If they elect not to attend a specialist NF1 clinic, they should be fully conversant with the problems that they might encounter. The minimum requirement for an asymptomatic adult is to have annual blood pressure measurement and to be aware of unusual symptoms, particularly the clinical features of malignant peripheral nerve sheath tumours and of spinal cord compression (see MPNST and neurological complications). Currently, the few specialist services for adults with NF1 are run by geneticists and neurologists. Further support is available through a small network of neurofibromatosis specialist advisors developed by the Neurofibromatosis Association and part funded by the National Health Service. The advisors have a nursing or social work background and act as patient advocates, providing support on medical, educational and emotional issues and coordinating with other professionals. An expansion of the specialist neurofibromatosis clinics and the specialist advisor network would enhance the provision of a cohesive pattern of care throughout the UK.
The manifestations of NF1 are widespread and affect many of the body systems (table 4)12
Café au lait patches and skin-fold freckling do not usually cause complications; however, some patients are distressed by the appearance of this pigmentation and may be helped by skin camouflage advice. There is no evidence to support the routine use of laser treatment for café au lait patches.
Hypopigmented macules may coexist with café au lait spots in NF1 and are found in a similar distribution.
Naevus anaemicus and benign cherry angiomas (Campbell de Morgan spots) are observed more frequently in NF1 than in the general population, irrespective of age. Juvenile xanthogranulomas are benign orange papules that appear transiently on the head and trunk in 1% of young children. It has been suggested that there is an increased risk of chronic myeloid leukaemia in children with NF1 and xanthogranulomas. However, routine haematological testing is not warranted in this group and a recent follow-up study did not reveal any haematological malignancies in 14 children with NF1 and xanthogranulomas.25
Neurofibromas are benign peripheral nerve sheath tumours that are focal cutaneous or subcutaneous, or diffuse or nodular plexiform lesions. Cutaneous neurofibromas are found in the majority of NF1 individuals, usually develop in the late teens or early twenties but occasionally emerge in early childhood.12,26 Initially, some lesions have a purplish tinge and may become pedunculated as they grow. The number of neurofibromas varies between individuals and within families.12,26 There have been no reports of these skin tumours undergoing malignant change but they often catch on clothing and cause cosmetic problems, transient stinging and itching. Irritation does not usually respond to antihistamines and the benefit of mast cell stabilisers is uncertain; excessive heat should be avoided and the use of emollients is advised.
Cutaneous neurofibromas can be removed if they cause any of the problems mentioned above. Referral to surgeons skilled in the removal of neurofibromas is advocated and plastic surgeons should be consulted for neurofibromas on the face and neck. There is no proven benefit of carbon dioxide laser treatment over surgical removal of troublesome neurofibromas but laser may be helpful for some small lesions. There is a risk of hypertrophic scarring and of recurrence of neurofibromas after removal.
Subcutaneous neurofibromas are evident on palpation of the skin, may be tender to touch and cause tingling in the distribution of the affected nerve.26 Malignant change rarely occurs and if removal is contemplated, expert advice should be sought from NF1 specialists or soft tissue tumour/peripheral nerve surgeons as removal occasionally results in neurological deficit.
Plexiform neurofibromas cause significant morbidity because they are diffuse, grow along the length of a nerve and may involve multiple nerve branches and plexi.26 The lesions can be nodular, and multiple discrete tumours may develop on nerve trunks. Plexiform neurofibromas infiltrate surrounding soft tissue and bony hypertrophy is evident in some instances.26 A large area of pigmentation often betrays the presence of a deep seated neurofibroma. The growth rate is unpredictable and there may be periods of rapid growth, particularly in adolescence, followed by periods of relative inactivity. Facial plexiform neurofibromas causing disfigurement appear during the first three years of life if they are to develop at all.12 Removal of benign plexiform neurofibromas is frequently very difficult due to encroachment of the tumour on surrounding structures and nerves and its inherent vascular nature. Life threatening haemorrhage can occur, particularly with facial plexiform neurofibromas. Expert advice from experienced soft tissue tumour or plastic surgeons is essential before removal. A number of agents (including farnesyl transferase inhibitors, antiangiogenesis drugs and fibroblast inhibitors) are being used in clinical trials to assess their therapeutic effect on growth of plexiform neurofibromas.27 Currently, there is insufficient evidence to support the use of any of these drugs in patients with symptomatic plexiform neurofibromas, and radiotherapy is contraindicated in benign tumours because of the risk of malignancy.
Malignant peripheral nerve sheath tumours
There is an 8–13% lifetime risk of developing MPNST in NF1, predominantly in individuals aged 20–35 years.28 These cancers are hard to detect, metastasise widely and often augur a poor prognosis.29 MPNST usually, but not invariably, arise in pre-existing plexiform neurofibromas. NF1 patients should seek an urgent expert opinion from specialist neurofibromatosis clinics or soft tissue tumour units if they develop any of the following in association with a subcutaneous or plexiform neurofibroma: persistent pain lasting for longer than a month or pain that disturbs sleep; new or unexplained neurological deficit or sphincter disturbance; alteration in the texture of a neurofibroma from soft to hard; and rapid increase in the size of a neurofibroma.29 Clinicians should be aware that occasionally symptoms arise from a plexiform neurofibroma that is not visible or palpable.
Individuals who have been treated with radiotherapy, have a personal or family history of cancer, optic pathway glioma, whole gene deletion, multiple subcutaneous neurofibromas or neurofibromatous neuropathy might have an increased risk of developing MPNST and require careful clinical monitoring.29–3318Fluorodeoxyglucose positron emission tomography allows the visualisation and quantification of glucose metabolism in cells and is a useful diagnostic tool in differentiating benign plexiform neurofibromas from MPNST.34 The aim of treatment is complete removal of the lesion with tumour free margins.29 Adjuvant radiotherapy has a role in treating MPNST larger than 5 cm, high grade lesions and incompletely excised tumours.29 Ifosfamide and doxorubicin are administered as palliative therapy in patients with metastatic disease and to reduce the size of a tumour with the aim of making it amenable to surgery.29
An association has been reported recently between glomus tumours and NF1.35 Glomus bodies are small, dermal, encapsulated arteriovenous anastomoses, commonest in the fingertips where they regulate peripheral blood flow and hence body temperature. The glomus tumour is usually solitary but multiple lesions have been observed in NF1 individuals.35 The lesion is located most frequently under the fingernail and presents with pain, cold sensitivity and excruciating very localised tenderness. The symptoms should be differentiated from those caused by subcutaneous neurofibromas and the treatment is local excision of the tumour.
Neurological examination should be undertaken during annual assessment. Any unexplained neurological signs and symptoms merit referral to a neurologist. Urgent advice is mandatory if individuals experience acute or progressive sensory disturbance, motor deficit and incoordination or sphincter disturbance which could be indicative of an intracranial lesion or spinal cord compression. Headaches on waking, morning vomiting and altered consciousness are suggestive of raised intracranial pressure and constitute a neurological emergency.
Neurological complications develop from tumours and malformations, including aqueduct stenosis.12,36 Skull deformity due to sphenoid wing dysplasia leads to pulsating exophthalmos as the temporal lobe herniates into the orbit.12 Severe scoliosis deforms the spine and results in cord compression and respiratory compromise.12 Neurological sequelae are the consequence of pressure on peripheral and spinal nerves and the spinal cord. Epilepsy is usually mild, occurs in approximately 6–7% of NF1 individuals and is likely to be related to an underlying cortical dysgenesis.37 Cerebrovascular disease, including carotid artery stenosis/occlusion, haemorrhage and aneurysm is part of the spectrum of NF1 vasculopathy.38 The causes of cognitive impairment, neurofibromatous neuropathy and multiple sclerosis in NF1 remain unclear.33,39,40
Cognitive problems and behavioural difficulties
Cognitive problems are the commonest neurological complication in NF1 individuals and usually present as an IQ in the low average range; severe intellectual deficit with an IQ <70 is rare.39,41,42 Specific learning problems have been observed in 30–60% of NF1 children.39,41–43 A child with a specific learning difficulty will fail to achieve his or her full academic potential, regardless of cultural or socioeconomic background, and in the absence of overt neurological, genetic or general medical problems. The disorder may be evident despite a normal or, more rarely, above average intelligence and includes clumsiness, reading/writing difficulties, visual spatial problems, working memory impairment and attention deficits. Behavioural problems comprise sleep disturbance, impaired socialisation, low self esteem and poor interpretation of social cues. There is an increased frequency of attention deficit hyperactivity and of autistic spectrum disorders.44,45
Ideally a detailed developmental assessment should be performed as soon as possible and definitely before school. Progress at school should be ascertained as part of the yearly assessment with enquiries about the child’s sleep patterns, ability to focus on an activity, distractibility, social interaction and fine and gross motor skills. NF1 children frequently have difficulty in dressing, holding a pencil, hopping, running and riding a bike compared with non-affected peers. Ligament laxity can contribute to delay in acquiring fine and gross motor skills. A special educational needs coordinator needs to be involved at an early stage and an educational statement should be prepared if appropriate. Close liaison between teachers, educational psychologists, occupational therapists and community paediatricians ensures that the child receives the optimum assessment and remedial support. Children with attention deficit frequently respond well to methylphenidate under experienced supervision, and cognitive behavioural therapy can be helpful.41,45 The benefit of the systematic use of methylphenidate in NF1 adults with attention deficit disorder has not been investigated.
The underlying pathogenesis of cognitive impairment in NF1 has not been determined and there is no consensus concerning the causative role of T2 hyperintensities in the brain.41,42,45 A recent study on a mouse model for NF1 has shown that attention deficits and visual spatial impairment are reversed by lovostatin, which is a specific inhibitor of HMG-CoA, the rate limiting enzyme in cholesterol biosynthesis.46 Current clinical studies are investigating the safety profile and tolerability of statin drugs in children with NF1. At present there is no justification for the use of these drugs in the treatment of cognitive impairment in NF1 individuals.
Although clumsiness improves with age, overall cognitive impairment remains stable in adulthood. Adults should be asked about their literacy and numeracy as impairment of these skills reduces clinic attendance and understanding of information about their condition. Referral to adult literacy classes might be appropriate in some instances. Clinic visits should be followed where possible by a telephone call to ascertain that the individual understands his/her care plan.
Central nervous system tumours
glioma is the predominant tumour type in NF1 and occurs in all parts of the nervous system, with a predilection for the optic pathways, brainstem and cerebellum.36 Brainstem gliomas manifest as diffuse or focal tumours and frequently have a more indolent course in NF1 than in the general population although occasionally they can behave aggressively.36,47 Symptomatic and progressive tumours are higher grade astrocytomas than pilocytic astrocytomas which have a more benign outcome.36,47 A recent study indicated that symptomatic tumours, those with adult onset and gliomas situated outside the optic pathway are associated with reduced survival. Meningiomas and vestibular schwannomas are the hallmark of NF2 and do not occur with increased frequency in NF1.
Optic pathway gliomas
Optic pathway gliomas (OPG) are grade 1, pilocytic astrocytomas and occur in about 15% of children with NF1.48 They are often asymptomatic and more indolent than their counterparts in the general population. However, some tumours produce impaired visual acuity, abnormal colour vision, visual field loss, squint, pupillary abnormalities, pale optic disc, proptosis and hypothalamic dysfunction. The risk of symptomatic OPG is greatest in children under 7 years, and older individuals rarely develop tumours that require medical intervention.48,49
Young children do not complain of visual impairment until it is advanced and sometimes only when they have bilateral visual loss. Parents need to be alert to possible pointers of visual problems: failure to pick up small toys and bumping into objects. Visual assessment is often problematic in young children and those with cognitive deficits. Recognition of visual acuity can be assessed at a developmental age of 3 years, colour vision at 5 years and visual fields at age 8 years. In the UK we have not yet detected an asymptomatic child on screening who later required treatment. None the less, the greatest risk of developing OPG is in young children, and those under 7 years should have annual visual acuity and fundoscopy looking for optic disc pallor and elevation. One baseline assessment of colour vision and visual fields should be undertaken when the child is mature enough to cope with the test. Brain MRI screening for OPG is not indicated as treatment is not required in the absence of progressive visual disturbance or proptosis. Diffusion tensor imaging has proved useful for detecting OPG in a mouse model and might be a valuable screening tool in children in the future.50
Specialist advice is essential for the management of OPG and therapy is usually with vincristine and cisplatinum.51 Occasionally surgery is warranted to deal with severe proptosis or to debulk extensive chiasmal gliomas. Radiotherapy is not advocated in young children because of potential second malignancy, neuropsychological, vascular and endocrine consequences. Rapamycin reduces astrocyte growth in vitro and might have a future therapeutic role in the management of OPG.52
Neurofibromas cause neurological symptoms through pressure on peripheral nerves, spinal nerve roots and on the spinal cord. Neurofibromas in the high cervical region appear to have a high risk of causing cord compression although the reason is not clear. None the less, many individuals with radiological cord compression have no neurological deficit and do not always require surgery. Hence referral to a tertiary centre is advocated for specialist advice.
Approximately 2% of individuals with NF1 develop bowing of the long bones, particularly the tibia and/or pseudarthrosis (a false joint in a long bone).12 The disorder is caused by an intrinsic defect of bone formation and bowing is apparent in the first few months of life. Fracture often occurs spontaneously or after trivial injury and there is delayed healing. Surgery is usually necessary and amputation of the affected limb is required in some cases. Infants should be examined for the presence of bowing of the long bone and clinicians should consider the possibility of pseudarthrosis when assessing young children for possible non-accidental injury.
NF1 children need yearly assessment of the spine, and individuals with clinical evidence of scoliosis should be referred for expert orthopaedic advice and imaging. NF1 causes disruption of bone maintenance and reduced bone mineral density.53 Scoliosis most commonly involves the lower cervical and upper thoracic spine and is either idiopathic or dystrophic.12,54 Dystrophic curves are associated with additional kyphosis and onset is earlier than in idiopathic cases. Dystrophic scoliosis typically involves 4–6 segments, causes distortion of the vertebral bodies and ribs and is rapidly progressive, requiring early spinal fusion. It can be associated with underlying plexiform neurofibroma and in severe cases results in respiratory compromise. Disturbed sleep and excessive snoring can indicate impaired respiratory function and people with severe scoliosis require regular pulmonary function tests. Surgeons conversant with NF1 should perform spinal surgery, as intrinsic abnormalities of bone make instrumentation difficult in this group. Clinicians need to be vigilant about the possibility of osteoporosis and have a low threshold for performing dexa scans.
Non-ossifying fibromas have been observed in association with NF1 and are benign lesions of the tubular long bones.55 Occasionally they cause pain and pathological fracture and need to be distinguished from malignant bone tumours.
Congenital heart disease, especially pulmonary stenosis, and hypertension are observed in NF1.38 A careful examination of the heart should be undertaken and if an unexplained murmur is present the child should be referred for a cardiology opinion and echocardiograph. Blood pressure must be checked annually and should be less than 140/90 mm Hg and less than 130/85 mm Hg in individuals with end organ damage or diabetes mellitus. If the blood pressure is found to be high during a clinic visit it should be checked three times in one month to verify the findings. Some adults are happy to monitor their own blood pressure using portable machines at home. Coarctation of the aorta can be detected by checking the blood pressure in the upper and lower limbs.
Renal artery stenosis occurs in approximately 2% of the NF1 population and the diagnosis should be considered in hypertensive children, young adults and pregnant women, refractory hypertension in older individuals and those with an abdominal bruit.12,38 Renal artery stenosis may be bilateral and is produced by stenosis of small or large vessels, aneurysm formation or extrinsic compression by an adjacent tumour. Individuals require evaluation at a specialist centre and treatment includes antihypertensives, percutaneous transluminal angioplasty and surgery. The outcome is variable as a result of recurrent stenosis following surgery.56
Phaeochromocytoma occurs in approximately 2% of NF1 individuals and about 12% of tumours are malignant.57 Clinical presentation includes hypertension/paroxysmal hypertension, palpitations, headache, dizziness or sweating. The 24 hour urinary catecholamines should be checked and if there are associated symptoms, it is advisable to commence the urine collection when the patient is symptomatic. Where there is a high index of suspicion, referral to specialist centres for evaluation and management is recommended. Treatment involves alpha and beta blockade before surgery and duodenal carcinoid may coexist with phaeochromocytoma.12 Treatment of essential hypertension is the same as in the general population.
Abdominal bloating, pain, dyspepsia, haemorrhage and constipation may denote a gastrointestinal neurofibroma. Carcinoid tumours have a predilection for the duodenum where they give rise to facial flushing, diarrhoea, right sided cardiac lesions, facial telangiectasiae and bronchoconstriction.58 Increased urinary levels of the serotonin metabolite 5-hydroxyindoleacetic acid confirm the diagnosis. Gastrointestinal stromal tumours, the commonest mesenchymal tumours of the gastrointestinal tract, have been observed recently in association with NF1.59 Patients present with anaemia and gastrointestinal bleeding but the majority of NF1 related tumours have a good prognosis.
Psychological problems stem from disfigurement caused by neurofibromas and from the complex and unpredictable nature of the disease. Symptoms of anxiety and depression are common and there are reported instances of attempted suicide, psychosis and sociopathic behaviour.39,60 Anxiety and depression usually respond to a combination of antidepressants and counselling. NF1 specialist advisors, psychiatrists and counsellors all play a role in managing psychological complications.
Contraception and pregnancy
Recent research has shown that 75% of neurofibromas carry progesterone receptors.61 However, there has been no confirmation that the combined oral contraceptive pill or the progesterone only pill contributes to neurofibroma growth.62 One study has reported an increased risk of perinatal complications in NF1, with a higher stillbirth rate, intrauterine growth retardation and caesarean section rate.63 Hence close liaison between the obstetrician and neurofibromatosis clinician is important when caring for pregnant individuals with NF1. During pregnancy, neurofibromas may grow in size and number and clinicians need to be aware of the risk of cord compression if spinal plexiform neurofibromas expand.64 Obstetricians should ensure pelvic neurofibromas do not impede delivery of the baby. Hypertension requires careful evaluation (see section on cardiovascular disease). Monitoring of anticonvulsant medication is essential and patients should be informed of the potential teratogenic effects of antiepileptic drugs and given advice on breastfeeding. Patients on anticonvulsants need folic acid 5 mg daily before conception, where possible, and vitamin K is administered to the mother for one month before delivery and to the infant at birth.
The child requires assessment at birth for possible early complications of NF1 and at least yearly review until the disease status is clarified. If there are no features by the age of 2 years, NF1 is unlikely but one final review at 5 years is advised.
An individual with NF1 has a 50% risk of passing on the condition to an offspring but the clinical problems cannot be predicted, even within families.18 When the complications that cause lifelong morbidity or early mortality are considered, the risk of having a severely affected child is about 1 in 12.
It is imperative to examine the parents for cutaneous stigmata or for Lisch nodules in the 50% of individuals who are the first in the family to be affected. Occasionally, a parent will be found to have a segmental/mosaic form of NF1. Although the parent might have few health problems he or she would have an increased risk of having a child with classical NF1. In the absence of clinical signs of NF1, the risk to the parent of having another child with NF1 is extremely small and less than 1%.
The NF1 gene mutation is found in approximately 85–95% of cases using a combination of molecular techniques, including dHPLC, direct sequencing, FISH, MLPA and array CGH.65,66 All Wales Medical Genetic Services at the Institute of Medical Genetics in Cardiff offers a clinical mutation testing service that takes approximately 8 weeks to produce a result. Mutational analysis of the entire NF1 coding region and flanking splice sites has been performed on 169 individuals in the past 2 years. Prenatal testing is possible by direct mutation testing of fetal DNA extracted from chorionic villous sampling or from amniocentesis. Alternatively, DNA markers in families with two or more affected individuals can be used for this purpose. However, many do not take up the option of prenatal assessment because of the inability to determine disease severity. Preimplantation genetic diagnosis is also available and gives a further option for couples wishing to avoid therapeutic termination of pregnancy.67 The diagnosis is ascertained using single cells removed from 3 day old embryos, and those that do not carry the NF1 mutation are transferred to the mother. Genetic counselling prior to conception is advised in all NF1 individuals.
SPECIALIST NF1 CLINICS
It is recommended that multidisciplinary neurofibromatosis clinics include a lead clinician, named consultants who are experts in their field and a specialist nurse. Ideally, the disciplines of neurology, paediatrics, genetics, ophthalmology, neurosurgery, plastic surgery, orthopaedics, soft tissue tumour surgery, psychiatry, dermatology, radiology and pathology should be represented. The role of the specialist clinic is to diagnose NF1 in difficult cases, monitor and manage complex disease, and educate and support the patient and family. The specialist service also provides a forum for clinical audit and academic interaction through multidisciplinary meetings and video conferencing.
Close collaboration between NF1 clinicians will facilitate a uniform approach to the diagnosis and management of NF1 and its complications. Reliable clinical and radiological assessment will be helpful in determining the value of potential therapeutic agents. Furthermore, the formation of a standardised UK database will facilitate the evaluation of care and long term response to treatment for this complex neurocutaneous disease.
We are grateful to the following for their advice and support: Robert Listernick, Linda Partridge, and The UK Neurofibromatosis Association.
Published Online First 14 November 2006
Competing interests: None.
Contact addresses: The Neurofibromatosis Association, 38 High St, Kingston on Thames KT1 1HL, UK; Tel 020 8439 1234, Fax 020 8439 1200; registered charity number 1078790. The Neurofibromatosis specialist advisors are based around the UK and can be contacted via the Neurofibromatosis Association.
For information on Genetic Units see: http://www.gig.org.uk/services.html
Neurofibromatosis specialist centres: Dr Rosalie Ferner, Department of Neurology, Guy’s Hospital, St Thomas St, London SE1 9RT, UK, Tel 020 7188 3970 (Guy’s and St Thomas’ specialist neurofibromatosis nurse: Melissa Vann-Blockley, Tel 0207 188-3971); Professor Gareth Evans and Dr Susan Huson, University Department of Medical Genetics and Regional Genetics Service, St Mary’s Hospital, Hathersage Rd, Manchester M13 0JH, UK, Tel 0161 276 6264.