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复合性嗜铬细胞瘤伴恶性外周神经鞘瘤:附 1 例报告及文献复习

Composite phaeochromocytoma with malignant peripheral nerve sheath tumour: A case report with summary of prior published cases.

机构信息

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.

出版信息

Indian J Pathol Microbiol. 2021 Jul-Sep;64(3):571-574. doi: 10.4103/IJPM.IJPM_524_20.

Abstract

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.

摘要

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。

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