{"title":"驾驭希恩综合征的无声发病:病例报告","authors":"Gurusha Bahl , Yashaswi Pathak , Md Sadique Hussain , Yoshita Gupta , Nikita Saraswat","doi":"10.1016/j.jecr.2024.100168","DOIUrl":null,"url":null,"abstract":"<div><p>Sheehan syndrome is a relatively rare complication of postpartum bleeding that mostly results from anterior pituitary impairment caused by ischemic necrosis. This report highlights a unique case of a 58-year-old female suffering from Sheehan syndrome presenting with recurrent episodes of vomiting, abdominal pain, and drowsiness. Laboratory investigations confirmed hyponatremia, hypoglycemia, hypocortisolism, and secondary hypothyroidism. MRI scans revealed a partially empty sella. Prompt treatment with sodium supplementation, levothyroxine, and hydrocortisone led to significant improvement in the patient's condition. This case underscores the critical importance of early recognition and comprehensive diagnostic approaches to optimize management. It also highlights the need for increased medical awareness and tailored treatments to enhance outcomes and prevent complications in Sheehan syndrome.</p></div>","PeriodicalId":56186,"journal":{"name":"Journal of Clinical and Translational Endocrinology: Case Reports","volume":"32 ","pages":"Article 100168"},"PeriodicalIF":0.0000,"publicationDate":"2024-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214624524000078/pdfft?md5=449454169450873f314e4962771daea1&pid=1-s2.0-S2214624524000078-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Navigating Sheehan syndrome's silent onset: A case report\",\"authors\":\"Gurusha Bahl , Yashaswi Pathak , Md Sadique Hussain , Yoshita Gupta , Nikita Saraswat\",\"doi\":\"10.1016/j.jecr.2024.100168\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Sheehan syndrome is a relatively rare complication of postpartum bleeding that mostly results from anterior pituitary impairment caused by ischemic necrosis. This report highlights a unique case of a 58-year-old female suffering from Sheehan syndrome presenting with recurrent episodes of vomiting, abdominal pain, and drowsiness. Laboratory investigations confirmed hyponatremia, hypoglycemia, hypocortisolism, and secondary hypothyroidism. MRI scans revealed a partially empty sella. Prompt treatment with sodium supplementation, levothyroxine, and hydrocortisone led to significant improvement in the patient's condition. This case underscores the critical importance of early recognition and comprehensive diagnostic approaches to optimize management. It also highlights the need for increased medical awareness and tailored treatments to enhance outcomes and prevent complications in Sheehan syndrome.</p></div>\",\"PeriodicalId\":56186,\"journal\":{\"name\":\"Journal of Clinical and Translational Endocrinology: Case Reports\",\"volume\":\"32 \",\"pages\":\"Article 100168\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2214624524000078/pdfft?md5=449454169450873f314e4962771daea1&pid=1-s2.0-S2214624524000078-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Clinical and Translational Endocrinology: Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2214624524000078\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical and Translational Endocrinology: Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214624524000078","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
Navigating Sheehan syndrome's silent onset: A case report
Sheehan syndrome is a relatively rare complication of postpartum bleeding that mostly results from anterior pituitary impairment caused by ischemic necrosis. This report highlights a unique case of a 58-year-old female suffering from Sheehan syndrome presenting with recurrent episodes of vomiting, abdominal pain, and drowsiness. Laboratory investigations confirmed hyponatremia, hypoglycemia, hypocortisolism, and secondary hypothyroidism. MRI scans revealed a partially empty sella. Prompt treatment with sodium supplementation, levothyroxine, and hydrocortisone led to significant improvement in the patient's condition. This case underscores the critical importance of early recognition and comprehensive diagnostic approaches to optimize management. It also highlights the need for increased medical awareness and tailored treatments to enhance outcomes and prevent complications in Sheehan syndrome.
期刊介绍:
The journal publishes case reports in a variety of disciplines in endocrinology, including diabetes, metabolic bone disease and osteoporosis, thyroid disease, pituitary and lipid disorders. Journal of Clinical & Translational Endocrinology Case Reports is an open access publication.