Department of Pathology, Institute of Post Graduate Medical Education and Research, Kolkata, India.
Department of Urology, Institute of Post Graduate Medical Education and Research, Kolkata, India.
Indian J Pathol Microbiol. 2021 Jul-Sep;64(3):571-574. doi: 10.4103/IJPM.IJPM_524_20.
Composite phaeochromocytomas (CP) are extremely uncommon adrenal medullary tumours where phaeochromocytoma coexists with another adrenal medullary tumour also of neural crest origin. CP includes combination of phaeochromocytoma along with a component of neuroblastoma, ganglioneuroblastoma, ganglioneuroma, benign nerve sheath tumour or a malignant peripheral nerve sheath tumour (MPNST). Here we describe the morphological and immunohistochemical details of a case of CP with MPNST in a 30 years old lady, without history of neurofibromatosis. Only 6 cases of CP with MPNST have been reported so far. We have tabulated a summary of these prior published cases of phaeochromocytoma with MPNST. To our knowledge, this is the first literature review describing the clinico-pathological characteristics of these rare tumours.
复合嗜铬细胞瘤(CP)是一种极为罕见的肾上腺髓质肿瘤,其中嗜铬细胞瘤与另一种源自神经嵴的肾上腺髓质肿瘤共存。CP 包括嗜铬细胞瘤与神经母细胞瘤、节细胞神经母细胞瘤、节细胞神经瘤、良性神经鞘瘤或恶性周围神经鞘瘤(MPNST)的组合。在此,我们描述了一位 30 岁女性 CP 伴 MPNST 的形态学和免疫组化细节,她没有神经纤维瘤病病史。迄今为止,仅报道了 6 例 CP 伴 MPNST。我们列出了这些先前发表的 CP 伴 MPNST 病例的总结。据我们所知,这是第一篇描述这些罕见肿瘤临床病理特征的文献综述。