neurofibromatoses/melasma

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Neurocutaneous melanosis, neurofibromatosis and spinal meningioma: an unusual association.

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The case of 38-year-old woman bearer of a congenital giant naevus "en pélerine" with numerous neurofibromas and other satellite naevi was reported: the patient was afflicted by spastic tetraparesis, more pronounced on the right side. MRIscan of the spine revealed the presence of a cervical spinal

Neurofibromatosis and neural crest neoplasms: primary acquired melanosis and malignant melanoma of the conjunctiva.

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With an occurrence of approximately 1 in 3000 births, von Recklinghausen neurofibromatosis (NF) is one of the most common inherited human disorders. NF is considered a neurocristopathy, a disorder of neural crest derived cells. One of the complications of NF is the development of neural crest

Conjunctival melanoma arising from primary acquired melanosis in a patient with neurofibromatosis type I.

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OBJECTIVE To describe a case of conjunctival malignant melanoma (MM) arising from primary acquired melanosis in a patient with neurofibromatosis type 1 (NF-1). METHODS Case report and literature review. RESULTS A 66-year-old woman with a history of NF-1 presented with extensive pigmentation of the

[A case from practice (345). 1. Suspicion of right-sided choroid melanoma--right-sided ocular melanosis. 2. Suspicion of type II neurofibromatosis--status following surgery of right-sided acoustic neurinoma in 1992].

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A study of palmar dermatoglyphics and palmar freckles.

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A study of palmar dermatoglyphics in genodermatoses was conducted in 219 probands and 100 control subjects by standard ink and roller method, during the period 1977-81 at Government General Hospital, Madras. A study of palmar dermatoglyphics in 20 probands with definite clinical and

Elephantiasis neuromatosa and Becker's melanosis.

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The most characteristic lesions of neurofibromatosis are the extremely large plexiform neurofibromas involving an entire extremity, which give rise to the condition known as elephantiasis neuromatosa. In this article, we present a patient who was diagnosed as elephantiasis neuromatosa with Becker's

Generalized melanoses and nonmelanotic pigmentations of the head and neck.

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The dentist is in a strategic position to evaluate early color changes of the head and neck. Certain oral and perioral changes of pigmentation are amenable to early diagnosis. Systemically acquired generalized melanoses and nonmelanotic color changes should be periodically reviewed by all examining

Dysphagia, melanosis, gastrointestinal stromal tumors and a germinal mutation of the KIT gene in an Argentine family.

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Gastrointestinal stromal tumors (GIST) are the most common mesenchymatous neoplasms of the human digestive tract. They locate preferentially in stomach, duodenum or small bowel. Usually sporadic, familial cases unrelated to neurofibromatosis may be due to germline mutations in KIT or PDGFRA. We

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