 |
 |

Familial Pheochromocytoma, Medullary Thyroid Carcinoma, and Parathyroid Adenomas
Edward Paloyan, MD;
Angelo Scanu, MD;
Francis H. Straus, MD;
Jack R. Pickleman, MD;
Daniel Paloyan, MD
JAMA. 1970;214(8):1443-1447.
Abstract
In a patient with bilateral malignant familial pheochromocytomas, medullary thyroid cancer, and parathyroid adenomas (Sipple's syndrome), high concentrations of calcitonin were assayed in the medullary cancer. A striking morphological similarity is noted between the medullary thyroid carcinoma and the metastases from the pheochromocytoma in this patient. The recently reported discovery of a calcitonin-like substance in the adrenal medulla and the morphological similarities between the pheochromocytomas' metastases and the calcitonin producing thyroid cancer are considered as evidence in support of the concept that this syndrome is a defect in a single (neuroectodermal) cell system.
Author Affiliations
From the departments of surgery (Drs. E. Paloyan, Pickleman, and D. Paloyan), pathology (Dr. Straus), and medicine (Dr. Scanu), University of Chicago Pritzker School of Medicine, and the Argonne Cancer Research Hospital, which is operated for the Atomic Energy Commission.
Footnotes
Reprint requests to 950 E 59th St, Chicago 60637 (Dr. E. Paloyan).
CiteULike Connotea Del.icio.us Digg Reddit Technorati Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
Uncommon Presentation of Pheochromocytoma: Case Studies
Grossman et al.
ANGIOLOGY 1985;36:759-765.
ABSTRACT
Pheochromocytoma Causing Excessive Parathyroid Hormone Production and Hypercalcemia
KUKREJA et al.
ANN INTERN MED 1973;79:838-840.
ABSTRACT
Iatrogenic Renal Hypertension: Two Unusual Complications of Surgery for Familial Pheochromocytoma
Castle
JAMA 1973;225:1085-1088.
ABSTRACT
Sipple's Syndrome: Medullary Thyroid Carcinoma, Pheochromocytoma, and Parathyroid Disease: Studies in a Large Family
KEISER et al.
ANN INTERN MED 1973;78:561-579.
ABSTRACT
Hypercalcemia and Familial Pheochromocytoma: Correction After Adrenalectomy
SWINTON et al.
ANN INTERN MED 1972;76:455-457.
ABSTRACT
|