Juarez D, Brown R W, Ostrowski M, Reardon M J, Lechago J, Truong L D
Department of Pathology, Baylor College of Medicine, and The Methodist Hospital, Houston, TX 77030, USA.
Arch Pathol Lab Med. 1999 Dec;123(12):1274-9. doi: 10.5858/1999-123-1274-PAWNC.
The coexistence of pheochromocytoma and other tumor types in a single adrenal gland has been rarely documented. This type of pheochromocytoma is designated "composite" or "mixed," depending on whether the pheochromocytoma and the nonpheochromocytoma components show the same embryologic origin. The nonpheochromocytoma components reported in the composite pheochromocytoma include ganglioneuroma, ganglioneuroblastoma, neuroblastoma, and malignant schwannoma. The components found in the mixed pheochromocytoma include adrenal cortical neoplasms and spindle cell sarcoma. We report a unique case of composite pheochromocytoma in which the nonpheochromocytoma element is a neuroendocrine carcinoma. The histologic and the immunohistochemical profiles of the 2 distinct components of this tumor were typical for those of pheochromocytoma and neuroendocrine carcinoma. This dual differentiation was also supported by ultrastructural findings. This case not only broadens the morphologic spectrum of composite pheochromocytoma but also provides some additional insight into the histogenesis of this rare but fascinating type of tumor.
单个肾上腺中嗜铬细胞瘤与其他肿瘤类型并存的情况鲜有文献记载。根据嗜铬细胞瘤与非嗜铬细胞瘤成分是否具有相同的胚胎学起源,这种类型的嗜铬细胞瘤被称为“复合性”或“混合性”。复合性嗜铬细胞瘤中报道的非嗜铬细胞瘤成分包括神经节神经瘤、神经节神经母细胞瘤、神经母细胞瘤和恶性神经鞘瘤。混合性嗜铬细胞瘤中发现的成分包括肾上腺皮质肿瘤和梭形细胞肉瘤。我们报告了一例独特的复合性嗜铬细胞瘤病例,其中非嗜铬细胞瘤成分是神经内分泌癌。该肿瘤两种不同成分的组织学和免疫组化特征对于嗜铬细胞瘤和神经内分泌癌来说是典型的。超微结构结果也支持这种双重分化。该病例不仅拓宽了复合性嗜铬细胞瘤的形态学谱,还为这种罕见但迷人的肿瘤类型的组织发生提供了一些额外的见解。