T ype 1 neurofibromatosis is an inherited multisystem neurocutaneous disease predisposing to tumors development. Serious skin and ophthalmologic complications, although rare, can occur throughout life. Furthermore in children, unawareness of early symptoms may delay diagnosis . We report the case of A.T. 8 years old, admitted for exophthalmosis and facial deformity dating back to the age of 2 years. The diagnosis of neurofibromatosis was suspected in the presence of light brown skin spots scattered all over the body and subcutaneous nodules. Ophthalmologic examination revealed bilateral exophthalmosis, eyelids neurofibromas, blepharoptosis, Lisch nodules, corneal edema, and optic atrophy. Head CT scan clarified the nature and the extent of ophthalmologic lesions. Treatment was symptomatic. Neurofibromatosis is rarely reported in children in our setting; it is probably under diagnosed. Clinicians should think of this diagnosis in presence of certain specific symptoms and make a clinical assessment.
Neurofibromatosis (NF) includes two autosomal dominant diseases: neurofibromatosis type 1 (NF1) or Von Recklinghausen disease and neurofibromatosis type 2 [
Clinical signs of NF1 are very diverse and increase in number and size as the individual grows older. The café au lait spots (CLS), visible at birth, are usually the first symptoms. As for eye complications, they can appear anywhere on the eye and at any age [
We report a case of neurofibromatosis type 1 in an 8 year old girl revealed by eye complications in the pediatric department of the Yalgado Ouédraogo Teaching Hospital in Ouagadougou, Burkina Faso. Informed consent was obtained from the patient’s family to report this case.
The eight years old girl was admitted at our department for eyelids blepharoptosis and facial deformity. The onset of symptoms goes back to the age of two years with gradual swelling of the cheeks and protrusion of the eyes. This has led to a series of consultations in their home region.
In October 2012, with the increasing eye protrusion and eyelids blepharoptosis, parents consulted for investigation.
The girl had a history of right upper eyelid tumor since birth. She was not known to have any other diseases other than the current abnormalities. She is second in a family of four siblings. Her growth (weight and height) and psychomotor development were normal. Clinical examination of the biological parents and siblings was unremarkable: no body spots, no deformity. The family had no history of similar diseases and there was no consanguinity between parents.
Examination of the head noted:
・ Bilateral eyelid swelling consisting of tender numbs with blepharoptosis more pronounced on the right eye. (
・ Bilateral exophthalmosis (
・ Hypertrophy of the right hemi face and facial asymmetry
・ Bilateral multinodular parotid swelling, compressing ear canals
Examination of the skin showed:
・ Light brown spots (café au lait spots), numerous, scattered all over the body, diameter > 5 mm (
・ Small hyperpigmented freckels (axillary freckles ) about 2 to 3 mm in diameter.
・ Tumors located on the back, some of them were only palpable, while others seemed to lift the skin above (subcutaneous neurofibromas ) as shown on
・ A soft sessile tumor about 3 cm diameter with hypertrichosis (plexiform neurofibroma), located on the back,
Ophthalmologic examination gave details of the eye lesions:
・ Bilateral plexiform neurofibromas of the upper eyelids
・ Lisch nodules (
・ A thinning of the sclera, corneal edema, and optic atrophy of the right eye. The left eye was healthy.
・ The intraocular pressure of the right eye was 41 cm and of the left eye 26 cm Hg (normal value: 10 - 20 cm Hg).The visual acuity was 4/10 on the right eye and 7/10 on the left eye.
Computed Tomography (CT scan) of the skull and brain specified the extent of the lesions (
・ Left temporal parenchymal calcifications ,
・ A bilateral grade III exophthalmosis,
・ Thickening of the initial portions of the optic nerves and eye muscles
Histological examination of a biopsy of the parotid mass confirmed the diagnosis of NF1. It showed fusiform cell cytoplasm and sometimes undulating pyknotic nucleus with myxoid or “onion bulb” territories compatible with neurofibroma.
Molecular biology in search of genetic anomalies could not be performed.
Treatment was symptomatic consisting of antibiotics, antiseptic and anti-inflammatory eye drops.
The course of the disease was marked by the gradual increase of blepharoptosis, of facial hypertrophy, and of the size of the plexiform neurofibroma on the back. One year later, the patient lost the sight of the right eye.
Diagnosis of neurofibromatosis at a very late stage with severe orbital complications, in our patient, is due to unawareness of the first symptoms of the disease in children.
The café au lait spots are usually the first symptoms of NF. They are often congenital and rarely appear after the age of two [
Neurofibromas rarely appear in early childhood, except plexiform neurofibromas which are often congenital and still can be seen before the age of five years [
Our patient had a lot of subcutaneous neurofibromas scattered on the right hemi face responsible for the hypertrophy. The plexiform neurofibromas, in their important form called “royal tumor” consist of skin and subcutaneous soft swellings with uneven consistency. The overlying skin is often thick and may be the site of hypertrichosis and a brown hyperpigmentation as in our patient. They predominate in the territory of the trigeminal nerve (eyelid and orbital) [
There was an important ophthalmologic involvement in our patient. Ophthalmologic manifestations may occur at an early age or later and eyelid disorders are the most common in NF1 [
Dysplasia of the sphenoid is the most common cause of exophthalmosis in children with enlargement of the orbit [
Lisch nodules are iris hamartomas which can sometimes be seen with the naked eye. They are pathognomonic of NF1 and are part of the diagnostic criteria [
A decrease in visual acuity usually affects the eye on the affected side of the head, sometimes associated with other abnormalities such as deterioration of visual field, or glaucoma [
Other ophthalmologic complications have also been described: thinning of the sclera, optic atrophy [
Genetic tests performed on the patient and his parents could have showed if this was de novo mutation or inherited transmission [
Surgery is the main treatment and must take into account the unpredictability of the disease [
In the end, the course of the disease is classically characterized by deterioration of symptoms during puberty or during an event such as pregnancy. Throughout life various tumors can occur [
Clinical diagnosis of NF1 is usually easy. In our study, health workers ignorance of early clinical signs certainly explains the long delay of diagnosis and numerous ophthalmologic manifestations observed. The unforeseeable development of NF1 warrants early diagnosis and regular monitoring throughout life. Molecular diagnostic methods would have determined the etiology of this condition and so consider genetic counseling. This study highlights the need for inter-disciplinary collaboration; without doubt surgery could have improved the quality of life of our patient.
CarolineYonaba,AichatouDjibo,ChantalZoungrana,AngèleKalmogho,OusseineDiallo,PatriceTapsoba,NoufounikounMéda,LudovicKam, (2015) Neurofibromatosis Type 1 Revealed by Ophthalmologic Complications: A Report of One Case in Ouagadougou, Burkina Faso. Open Journal of Pediatrics,05,290-295. doi: 10.4236/ojped.2015.54044