{"title":"子宫肌瘤黏液性病:一例罕见的原发性不孕患者","authors":"Nilam Subedi, P. Pant, A. Ghimire","doi":"10.3126/GMJ.V1I1.22420","DOIUrl":null,"url":null,"abstract":"Myxoid mesenchymal lesions of the uterus are generally restricted to tumors. Myometrial myxoidosis is a rare benign tumor of the uterus. We report a case of myometrial myxoidosis diagnosed postoperatively with histopathological report in a 27-year-old female with primary subfertility who had undergone myomectomy and adenomyomectomy. On gross examination the tumor was 13.5x8x2.5 cm in size. Microscopically, it showed interlacing bundles of smooth muscles intersecting each other. Sections from separate tissue showed muscle fascicles which were separated by abundant extracellular mucin producing a striking myxoid appearance (myxoidosis). \nOnly few cases of myometrial myxoidosis have been reported in literature. Of them, some were associated with lupus erythematosus and some with neurofibromatosis.","PeriodicalId":314361,"journal":{"name":"Grande Medical Journal","volume":"108 1-2 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Myometrial myxoidosis: A rare case seen in a patient of primary subfertility\",\"authors\":\"Nilam Subedi, P. Pant, A. Ghimire\",\"doi\":\"10.3126/GMJ.V1I1.22420\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Myxoid mesenchymal lesions of the uterus are generally restricted to tumors. Myometrial myxoidosis is a rare benign tumor of the uterus. We report a case of myometrial myxoidosis diagnosed postoperatively with histopathological report in a 27-year-old female with primary subfertility who had undergone myomectomy and adenomyomectomy. On gross examination the tumor was 13.5x8x2.5 cm in size. Microscopically, it showed interlacing bundles of smooth muscles intersecting each other. Sections from separate tissue showed muscle fascicles which were separated by abundant extracellular mucin producing a striking myxoid appearance (myxoidosis). \\nOnly few cases of myometrial myxoidosis have been reported in literature. Of them, some were associated with lupus erythematosus and some with neurofibromatosis.\",\"PeriodicalId\":314361,\"journal\":{\"name\":\"Grande Medical Journal\",\"volume\":\"108 1-2 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-01-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Grande Medical Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3126/GMJ.V1I1.22420\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Grande Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3126/GMJ.V1I1.22420","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Myometrial myxoidosis: A rare case seen in a patient of primary subfertility
Myxoid mesenchymal lesions of the uterus are generally restricted to tumors. Myometrial myxoidosis is a rare benign tumor of the uterus. We report a case of myometrial myxoidosis diagnosed postoperatively with histopathological report in a 27-year-old female with primary subfertility who had undergone myomectomy and adenomyomectomy. On gross examination the tumor was 13.5x8x2.5 cm in size. Microscopically, it showed interlacing bundles of smooth muscles intersecting each other. Sections from separate tissue showed muscle fascicles which were separated by abundant extracellular mucin producing a striking myxoid appearance (myxoidosis).
Only few cases of myometrial myxoidosis have been reported in literature. Of them, some were associated with lupus erythematosus and some with neurofibromatosis.