Gupta R, Sharma A, Arora R, Vijayaraghavan M
Department of Pathology, All India Institute of Medical Sciences, New Delhi, India.
J Clin Pathol. 2009 Jul;62(7):659-61. doi: 10.1136/jcp.2009.064790.
The coexistence of adrenal phaeochromocytoma with non-chromaffin tumours is a rare fascinating occurrence. This category of tumours is subdivided into "composite" and "mixed". The coexistence of adrenal phaeochromocytoma with a malignant Triton tumour does not appear to have been described in the available literature so far. A unique case of composite phaeochromocytoma in a 26-year-old male patient, where the non-chromaffin component was a malignant Triton tumour composed of peripheral nerve sheath tumour and skeletal muscle differentiation, is reported. This admixture was confirmed with immunohistochemical pattern of expression. This is the first case of such a phenomenon in a composite phaeochromocytoma. The present case further widens the histomorphological range of composite phaeochromocytoma of the adrenal gland, which the histopathologist should be aware of. Since the prognosis of composite phaeochromocytoma with malignant nerve sheath tumour would be determined by the nerve sheath component, recognition of this tumour is imperative.
肾上腺嗜铬细胞瘤与非嗜铬细胞瘤共存是一种罕见且引人关注的情况。这类肿瘤可细分为“复合型”和“混合型”。目前在现有文献中,肾上腺嗜铬细胞瘤与恶性蝾螈瘤共存的情况似乎尚未见报道。本文报告了一例26岁男性患者的复合型嗜铬细胞瘤,其非嗜铬成分是一种由外周神经鞘瘤和骨骼肌分化构成的恶性蝾螈瘤。通过免疫组化表达模式证实了这种混合情况。这是复合型嗜铬细胞瘤中首例出现这种现象的病例。该病例进一步拓宽了肾上腺复合型嗜铬细胞瘤的组织形态学范围,病理学家应予以关注。由于伴有恶性神经鞘瘤的复合型嗜铬细胞瘤的预后将由神经鞘成分决定,因此识别这类肿瘤至关重要。