{"title":"内分泌病理诊断的挑战:三个病例突出内分泌腺的潜在诊断缺陷","authors":"Dinuke Shehan de Silva, Tristan Rutland","doi":"10.1016/j.mpdhp.2025.06.002","DOIUrl":null,"url":null,"abstract":"<div><div><span><span><span><span>This article presents three cases illustrating potential diagnostic pitfalls in endocrine gland neoplasms<span>. The first case is of a 69 year old male with a new diagnosis of multiple myeloma<span> along with radiologically detected lung and bilateral adrenal gland masses. Biopsies revealed a poorly differentiated </span></span></span>lung adenocarcinoma that was positive for neuroendocrine markers and CD138, which can lead to confusion with a primary </span>pheochromocytoma<span> and plasma cell neoplasm, respectively. The second case presented is of a 62 year old male with a lesion in the right adrenal gland which on histology was revealed to be a metastatic </span></span>clear cell renal cell carcinoma<span> (ccRCC) that occurred 14 years after resection of the primary. This case highlights that ccRCC metastases<span> can occur many years after the initial excision. The case also highlights the differentials for clear cell tumours of the adrenal glands which includes </span></span></span>adrenocortical adenoma<span><span>. The final case presented is of a 63 year old male with a past history of Merkel cell carcinoma with a large left sided </span>adrenal gland metastasis<span>. Core biopsies revealed a basaloid tumour positive for CK20 and neuroendocrine markers, confirming a diagnosis of metastatic Merkel cell carcinoma. Metastatic Merkel cell carcinoma may be mistaken for pheochromocytoma due to co-expression of neuroendocrine markers and both having a superficial basaloid appearance.</span></span></div></div>","PeriodicalId":39961,"journal":{"name":"Diagnostic Histopathology","volume":"31 9","pages":"Pages 506-513"},"PeriodicalIF":0.0000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Diagnostic challenges of endocrine pathology: three cases highlighting potential diagnostic pitfalls in endocrine glands\",\"authors\":\"Dinuke Shehan de Silva, Tristan Rutland\",\"doi\":\"10.1016/j.mpdhp.2025.06.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><span><span><span><span>This article presents three cases illustrating potential diagnostic pitfalls in endocrine gland neoplasms<span>. The first case is of a 69 year old male with a new diagnosis of multiple myeloma<span> along with radiologically detected lung and bilateral adrenal gland masses. Biopsies revealed a poorly differentiated </span></span></span>lung adenocarcinoma that was positive for neuroendocrine markers and CD138, which can lead to confusion with a primary </span>pheochromocytoma<span> and plasma cell neoplasm, respectively. The second case presented is of a 62 year old male with a lesion in the right adrenal gland which on histology was revealed to be a metastatic </span></span>clear cell renal cell carcinoma<span> (ccRCC) that occurred 14 years after resection of the primary. This case highlights that ccRCC metastases<span> can occur many years after the initial excision. The case also highlights the differentials for clear cell tumours of the adrenal glands which includes </span></span></span>adrenocortical adenoma<span><span>. The final case presented is of a 63 year old male with a past history of Merkel cell carcinoma with a large left sided </span>adrenal gland metastasis<span>. Core biopsies revealed a basaloid tumour positive for CK20 and neuroendocrine markers, confirming a diagnosis of metastatic Merkel cell carcinoma. Metastatic Merkel cell carcinoma may be mistaken for pheochromocytoma due to co-expression of neuroendocrine markers and both having a superficial basaloid appearance.</span></span></div></div>\",\"PeriodicalId\":39961,\"journal\":{\"name\":\"Diagnostic Histopathology\",\"volume\":\"31 9\",\"pages\":\"Pages 506-513\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Diagnostic Histopathology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1756231725001069\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Diagnostic Histopathology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1756231725001069","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Diagnostic challenges of endocrine pathology: three cases highlighting potential diagnostic pitfalls in endocrine glands
This article presents three cases illustrating potential diagnostic pitfalls in endocrine gland neoplasms. The first case is of a 69 year old male with a new diagnosis of multiple myeloma along with radiologically detected lung and bilateral adrenal gland masses. Biopsies revealed a poorly differentiated lung adenocarcinoma that was positive for neuroendocrine markers and CD138, which can lead to confusion with a primary pheochromocytoma and plasma cell neoplasm, respectively. The second case presented is of a 62 year old male with a lesion in the right adrenal gland which on histology was revealed to be a metastatic clear cell renal cell carcinoma (ccRCC) that occurred 14 years after resection of the primary. This case highlights that ccRCC metastases can occur many years after the initial excision. The case also highlights the differentials for clear cell tumours of the adrenal glands which includes adrenocortical adenoma. The final case presented is of a 63 year old male with a past history of Merkel cell carcinoma with a large left sided adrenal gland metastasis. Core biopsies revealed a basaloid tumour positive for CK20 and neuroendocrine markers, confirming a diagnosis of metastatic Merkel cell carcinoma. Metastatic Merkel cell carcinoma may be mistaken for pheochromocytoma due to co-expression of neuroendocrine markers and both having a superficial basaloid appearance.
期刊介绍:
This monthly review journal aims to provide the practising diagnostic pathologist and trainee pathologist with up-to-date reviews on histopathology and cytology and related technical advances. Each issue contains invited articles on a variety of topics from experts in the field and includes a mini-symposium exploring one subject in greater depth. Articles consist of system-based, disease-based reviews and advances in technology. They update the readers on day-to-day diagnostic work and keep them informed of important new developments. An additional feature is the short section devoted to hypotheses; these have been refereed. There is also a correspondence section.