The Korean Journal of Internal Medicine · 2000 · 14 citations · 9 references
MedicinePathologySurgeryEndocrine OncologyNeoplasiaTumor PathologyAdrenal TumorsEndocrine Tumor PathologyEndocrine TumorsHormone-secreting TumorsMediastinal TumorsNeuroendocrine TumorsAnterior Mediastinal LesionsEctopic Hormone ProductionGeneralized EdemaImmunohistochemical DetectionImmunohistochemical MarkersMediastinal ParagangliomaParaganglioma PathologySupraclavicular Lymph Nodes
Paragangliomas are unusual neuroendocrine cell tumors arising from paraganglia, of which ACTH-secreting cases in the mediastinum are extremely rare. A 51-year-old woman was admitted for generalized edema and weakness which began 5 months ago. Chest X-ray and CT scan revealed a tumor mass in the anterior mediastinum. The plasma cortisol and ACTH levels were very high. Other sources secreting ACTH, except mediastinal mass, were not found. Surgical excision of mediastinal mass and left supraclavicular lymph node was performed. The postoperative microscopic finding and immunohistochemical staining revealed organoid tumor cell nests (zellballen) and S-100 protein positive sustentacular cells which are characteristics of paraganglioma. This was thus a case of Cushing's syndrome resulting from ectopic ACTH production in anterior mediastinal paraganglioma.
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Diagnosis and management of catecholamine secreting glomus tumors.
Mitchell K. Schwaber, Michael E. Glasscock, C. Gary Jackson et al. · The Laryngoscope · 1984 · 145 citations
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César A. Moran, Nancy F. Fishback, Michael N. Koss et al. · Cancer · 1993 · 95 citations · Full text
The location of middle mediastinal pheochromocytomas
Brahm Shapiro, Victor Kalff, Jerry V. Glowniak et al. · Journal of Thoracic and Cardiovascular Surgery · 1984 · 91 citations
Medicine, Endocrinology, Pathology +11