Abdominal neurofibromatosis
نویسندگان
چکیده
منابع مشابه
Abdominal mass in a 19-year-old with neurofibromatosis.
Accepted 10 May 1996 A 19-year-old white man with known von Recklinghausen's neurofibromatosis developed anorexia and abdominal pain associated with a mobile lower abdominal mass. Characteristic cafeau-lait spots and subcutaneous neurofibromas were present. Other features associated with von Recklinghausen's disease' -I included mental retardation, a history ofheadaches and seizures, and scolio...
متن کاملNeurofibromatosis
Neurofibromatosis (NF) is an inherited disorder characterized by the development of a wide variety of clinical manifestations, including characteristic "freckle-like" pigmentations (cafe au lait spots) that develop in infancy, followed by skin tumors that may vary widely in size, number, and distribution. In addition to skin tumors, bone, neurologic, and endocrine abnormalities are common. NF i...
متن کاملA Case of a Patient with Neurofibromatosis Type I Presenting with Abdominal Pain.
Answer: D A 56-year-old gentleman presented to the emergency department after sustaining a fall secondary to an episode of giddiness. He was noted to be hypotensive in the ambulance and subsequently gave a history of non-specific abdominal pain for duration of 1 week. Imaging studies including an abdominal radiograph and a computed tomography (CT) of the abdomen and pelvis (CTAP) were performed...
متن کاملSolitary neurofibroma in the abdominal wall of a patient without neurofibromatosis: case report.
INTRODUCTION Solitary neurofibromas are benign tumors, often the manifestation of neurofibromatosis, and reflect a hereditary pathology with several variants. The clinical manifestations of solitary neurofibromas change according to their location and can generate a variety of symptoms. Usually, solitary neurofibromas are located in the skin and rarely in other places. Surgical removal is the o...
متن کاملSegmental Neurofibromatosis Type 1, a Rare Variant of Neurofibromatosis: Report of Two Cases
Segmental neurofibromatosis type I (SNF-I) is a rare variant of neurofibromatosis (NF). It is classified as NF type V and defined as cafe'-au-lait macules and/or neurofibromas in a single ,unilateral segment of the body .We report two cases with SNF-I with striking similar manifestations.
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ژورنال
عنوان ژورنال: Journal of the Royal Society of Medicine
سال: 1999
ISSN: 0141-0768,1758-1095
DOI: 10.1177/014107689909201115