D. Juarez et al., Pheochromocytoma associated with neuroendocrine carcinoma - A new type of composite pheochromocytoma, ARCH PATH L, 123(12), 1999, pp. 1274-1279
Citations number
32
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
The coexistence of pheochromocytoma and other tumor types in a single adren
al gland has been rarely documented. This type of pheochromocytoma is desig
nated "composite" or "mixed," depending on whether the pheochromocytoma and
the nonpheochromocytoma components show the same embryologic origin. The n
onpheochromocytoma components reported in the composite pheochromocytoma in
clude ganglioneuroma, ganglioneuroblastoma, neuroblastoma, and malignant sc
hwannoma. The components found in the mixed pheochromocytoma include adrena
l cortical neoplasms and spindle cell sarcoma. We report a unique case of c
omposite pheochromocytoma in which the nonpheochromocytoma element is a neu
roendocrine carcinoma. The histologic and the immunohistochemical profiles
of the 2 distinct components of this tumor were typical for those of pheoch
romocytoma and neuroendocrine carcinoma. This dual differentiation was also
supported by ultrastructural findings. This case not only broadens the mor
phologic spectrum of composite pheochromocytoma but also provides some addi
tional insight into the histogenesis of this rare but fascinating type of t
umor.