{"title":"子宫外:诊断难题为良性转移性平滑肌瘤病伴腹膜后和肺受累。","authors":"Supriya Adiody, Vishnu Narayanan S, Kanjoor Deepthi Damodaran Nair, Sareena Gilvaz, Aiswarya Pradeep","doi":"10.1136/bcr-2025-268274","DOIUrl":null,"url":null,"abstract":"<p><p>Benign metastasising leiomyomatosis (BML) is a rare entity characterised by the spread of benign smooth muscle cells, most commonly from uterine leiomyomas, to distant sites-most often the lungs. We present a case of a woman in her 40s who presented with abnormal uterine bleeding. Initial imaging revealed multiple uterine fibroids, a retroperitoneal mass mimicking gastrointestinal stromal tumour. HRCT chest showed thin-walled cystic lung nodules creating a suspicion of lymphangioleiomyomatosis (LAM). Following total abdominal hysterectomy with bilateral salpingo-oophorectomy and excision of the retroperitoneal lesion, histopathology and immunohistochemistry (IHC) confirmed a spindle cell tumour probably leiomyoma. Although the lung lesions were initially suggestive of LAM, the IHC study of the retroperitoneal lesion showed negative HMB-45 staining, and the genetic study also ruled out tuberous sclerosis complex mutations. Hence, we finally came to the diagnosis of BML. This case highlights the diagnostic challenges posed by cystic lung lesions in BML and underscores the need for a multidisciplinary approach incorporating histology, IHC and genetic testing to differentiate BML from mimickers like LAM or low-grade leiomyosarcoma.</p>","PeriodicalId":9080,"journal":{"name":"BMJ Case Reports","volume":"18 9","pages":""},"PeriodicalIF":0.6000,"publicationDate":"2025-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Beyond the uterus: diagnostic puzzle unravelled as benign metastasising leiomyomatosis with retroperitoneal and pulmonary involvement.\",\"authors\":\"Supriya Adiody, Vishnu Narayanan S, Kanjoor Deepthi Damodaran Nair, Sareena Gilvaz, Aiswarya Pradeep\",\"doi\":\"10.1136/bcr-2025-268274\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Benign metastasising leiomyomatosis (BML) is a rare entity characterised by the spread of benign smooth muscle cells, most commonly from uterine leiomyomas, to distant sites-most often the lungs. We present a case of a woman in her 40s who presented with abnormal uterine bleeding. Initial imaging revealed multiple uterine fibroids, a retroperitoneal mass mimicking gastrointestinal stromal tumour. HRCT chest showed thin-walled cystic lung nodules creating a suspicion of lymphangioleiomyomatosis (LAM). Following total abdominal hysterectomy with bilateral salpingo-oophorectomy and excision of the retroperitoneal lesion, histopathology and immunohistochemistry (IHC) confirmed a spindle cell tumour probably leiomyoma. Although the lung lesions were initially suggestive of LAM, the IHC study of the retroperitoneal lesion showed negative HMB-45 staining, and the genetic study also ruled out tuberous sclerosis complex mutations. Hence, we finally came to the diagnosis of BML. This case highlights the diagnostic challenges posed by cystic lung lesions in BML and underscores the need for a multidisciplinary approach incorporating histology, IHC and genetic testing to differentiate BML from mimickers like LAM or low-grade leiomyosarcoma.</p>\",\"PeriodicalId\":9080,\"journal\":{\"name\":\"BMJ Case Reports\",\"volume\":\"18 9\",\"pages\":\"\"},\"PeriodicalIF\":0.6000,\"publicationDate\":\"2025-09-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMJ Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1136/bcr-2025-268274\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMJ Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1136/bcr-2025-268274","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
Beyond the uterus: diagnostic puzzle unravelled as benign metastasising leiomyomatosis with retroperitoneal and pulmonary involvement.
Benign metastasising leiomyomatosis (BML) is a rare entity characterised by the spread of benign smooth muscle cells, most commonly from uterine leiomyomas, to distant sites-most often the lungs. We present a case of a woman in her 40s who presented with abnormal uterine bleeding. Initial imaging revealed multiple uterine fibroids, a retroperitoneal mass mimicking gastrointestinal stromal tumour. HRCT chest showed thin-walled cystic lung nodules creating a suspicion of lymphangioleiomyomatosis (LAM). Following total abdominal hysterectomy with bilateral salpingo-oophorectomy and excision of the retroperitoneal lesion, histopathology and immunohistochemistry (IHC) confirmed a spindle cell tumour probably leiomyoma. Although the lung lesions were initially suggestive of LAM, the IHC study of the retroperitoneal lesion showed negative HMB-45 staining, and the genetic study also ruled out tuberous sclerosis complex mutations. Hence, we finally came to the diagnosis of BML. This case highlights the diagnostic challenges posed by cystic lung lesions in BML and underscores the need for a multidisciplinary approach incorporating histology, IHC and genetic testing to differentiate BML from mimickers like LAM or low-grade leiomyosarcoma.
期刊介绍:
BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.