Title: Neurofibromatosis and
Pheochromocytoma. Multiple
endocrine neoplasm type III. Report of a case.
Authors:
Pizarro, A: Department of
Pathology. Nayarit Autonomous University, México
Díaz, R: Department of
Pathology. Nayarit Autonomous University, México
Contact Person: Alberto
G Pizarro (rediegal@homonet.com.mx)
Abstract
Clinical history: Woman 38 old
years, with illness of neurofibromatosis
generalized of 20 years of evolution. One of them
wicked four years ago. she begin clinical report
of intense sudden prechordial pain , dyspnea of
few efforts, tachycardia, arterial hypertension
160-120 mmhg, hypothermia. She presents heart
failure and death in 6 hours. The clinical
diagnosis was acute infart of the myocardium.
Autopsy: WE identify multiple
cutaneous neurofibromas, two in spinal cord and
two in stomach. We identified a pheochromocytoma
of right adrenal , an aortic paraganglioma , an
ovarian tecofibroma. The heart without thrombosis
of coronary arteries and multiple focal necrosis.
Pathological diagnosis:
multiple sistemic Neurofibromatosis +
pheochromocytoma. multiple endocrine neoplasia
type III.
WE analized clinic and
pathology report of NEM type III.
Poster Number PApizarro0189
Keywords:
pheochromocytoma, NEM III,
neurofibromatosis, neoplasia, tumours.
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