Emergencies Caused by Pheochromocytoma, Neuroblastoma, or Ganglioneuroma

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منابع مشابه

Extra-adrenal composite pheochromocytoma-ganglioneuroma.

Composite tumors containing pheochromocytoma and ganglioneuroma are rare tumors typically arising in the adrenal glands. Very few were reported outside of the adrenals. We present the case of a middle-aged woman with a retroperitoneal mass that was discovered when she complained of local signs of compression and systemic signs of catecholamine hypersecretion. On pathology the mass was composed ...

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REGRESSION OF METASTATIC NEUROBLASTOMA TO GANGLIONEUROMA

The spontaneous regression of neuroblastoma to ganlioneuroma is a rare occurrence. Reviewing the literature, we found no more than 12casesreported.'•2.9.,o.'4.1s We report a case of metastatic neuroblastoma of multifocal skeletal and soft tissue areas with gross deformities which regressed to ganglioneuroma, with good prognosis.

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regression of metastatic neuroblastoma to ganglioneuroma

the spontaneous regression of neuroblastoma to ganlioneuroma is a rare occurrence. reviewing the literature, we found no more than 12casesreported.'•2.9.,o.'4.1s we report a case of metastatic neuroblastoma of multifocal skeletal and soft tissue areas with gross deformities which regressed to ganglioneuroma, with good prognosis.

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Childhood neuroblastoma masquerading as pheochromocytoma: case report.

Neuroblastoma is the most common extracranial solid tumor in children. Mild hypertension is a frequent symptom, presumably an effect of catecholamines that tumors release. Reported herein is the rare occurrence of severe hypertension and subsequent heart failure attributable to adrenal gland neuroblastoma. A 3-year-old boy presented with anterior chest wall protrusion. Physical examination reve...

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Survivors of neuroblastoma and ganglioneuroma and their families.

The main purpose of this study was to see if the offspring of surviving neuroblastoma, ganglioneuroblastoma, or ganglioneuroma patients have themselves a risk for developing tumours. No such risk was found. There was a total of 45 liveborn children who were all healthy. These children have passed through about 37 lifetimes of risk for developing neuroblastoma and about six lifetimes of risk for...

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ژورنال

عنوان ژورنال: Endocrinology and Metabolism Clinics of North America

سال: 2006

ISSN: 0889-8529

DOI: 10.1016/j.ecl.2006.09.014