Boaz Elad, Wojciech Rzechorzek, Kelly Axsom, Justin Fried, Farhana Latif, Adil Yunis, Carolyn Hennecken, Rubin Salazar, Kyung T Oh, David L Diuguid, Andrew H Lipsky, Ron S Gejman, Gabriel Sayer, Nir Uriel, Dor Lotan
{"title":"病例报告:心脏移植中嗜血细胞淋巴组织细胞增多症的独特病例。","authors":"Boaz Elad, Wojciech Rzechorzek, Kelly Axsom, Justin Fried, Farhana Latif, Adil Yunis, Carolyn Hennecken, Rubin Salazar, Kyung T Oh, David L Diuguid, Andrew H Lipsky, Ron S Gejman, Gabriel Sayer, Nir Uriel, Dor Lotan","doi":"10.1016/j.transproceed.2025.02.021","DOIUrl":null,"url":null,"abstract":"<p><p>Hemophagocytic lymphohistiocytosis (HLH) is a rare and deadly disease that presents significant diagnostic challenges. The complexity of diagnosis and treatment is further increased among transplant recipients, yet reports on solid organ transplants, and specifically heart transplant recipients, remain scarce. Herein, we elucidate the diagnostic journey, clinical evolution, and therapeutic approach undertaken for a heart transplant recipient afflicted with hemophagocytic lymphohistiocytosis, followed by a review of the literature.</p>","PeriodicalId":94258,"journal":{"name":"Transplantation proceedings","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Case Report: A Unique Case of Hemophagocytic Lymphohistiocytosis in Heart Transplant.\",\"authors\":\"Boaz Elad, Wojciech Rzechorzek, Kelly Axsom, Justin Fried, Farhana Latif, Adil Yunis, Carolyn Hennecken, Rubin Salazar, Kyung T Oh, David L Diuguid, Andrew H Lipsky, Ron S Gejman, Gabriel Sayer, Nir Uriel, Dor Lotan\",\"doi\":\"10.1016/j.transproceed.2025.02.021\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Hemophagocytic lymphohistiocytosis (HLH) is a rare and deadly disease that presents significant diagnostic challenges. The complexity of diagnosis and treatment is further increased among transplant recipients, yet reports on solid organ transplants, and specifically heart transplant recipients, remain scarce. Herein, we elucidate the diagnostic journey, clinical evolution, and therapeutic approach undertaken for a heart transplant recipient afflicted with hemophagocytic lymphohistiocytosis, followed by a review of the literature.</p>\",\"PeriodicalId\":94258,\"journal\":{\"name\":\"Transplantation proceedings\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-02-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Transplantation proceedings\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1016/j.transproceed.2025.02.021\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transplantation proceedings","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.transproceed.2025.02.021","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Case Report: A Unique Case of Hemophagocytic Lymphohistiocytosis in Heart Transplant.
Hemophagocytic lymphohistiocytosis (HLH) is a rare and deadly disease that presents significant diagnostic challenges. The complexity of diagnosis and treatment is further increased among transplant recipients, yet reports on solid organ transplants, and specifically heart transplant recipients, remain scarce. Herein, we elucidate the diagnostic journey, clinical evolution, and therapeutic approach undertaken for a heart transplant recipient afflicted with hemophagocytic lymphohistiocytosis, followed by a review of the literature.