Hemophagocytic Lymphohistiocytosis in Cutaneous T-Cell Lymphoma
Sign Up to like & getrecommendations! Published in 2018 at "JAMA Dermatology"
DOI: 10.1001/jamadermatol.2018.1264
Abstract: Importance Hemophagocytic lymphohistiocytosis (HLH) has been reported as a serious complication of cutaneous T-cell lymphoma (CTCL). Despite available diagnostic guidelines, it remains a diagnostic and therapeutic challenge in this patient population. Objectives To examine the… read more here.
Keywords: cutaneous cell; hemophagocytic lymphohistiocytosis; cell; hlh ... See more keywords
High prevalence of osteonecrosis among the hemophagocytic lymphohistiocytosis population: Single institution 10‐year retrospective data review
Sign Up to like & getrecommendations! Published in 2017 at "American Journal of Hematology"
DOI: 10.1002/ajh.24828
Abstract: To the Editor: Hemophagocytic lymphohistiocytosis (HLH) is a rare disorder that is characterized by overactive natural-killer and cytotoxic T cells that improperly trigger macrophages and subsequently leads to hemophagocytosis in bone marrow, spleen, liver, and… read more here.
Keywords: osteonecrosis; secondary hlh; diagnosis; prevalence ... See more keywords
Establishment and characterization of a novel Hodgkin lymphoma cell line, AM‐HLH, carrying the Epstein‐Barr virus genome integrated into the host chromosome
Sign Up to like & getrecommendations! Published in 2017 at "Hematological Oncology"
DOI: 10.1002/hon.2369
Abstract: We describe the establishment and characterization of a cell line, AM‐HLH, obtained from a patient with Epstein‐Barr virus–positive (EBV+) nodular sclerosis–type Hodgkin lymphoma (HL). The cells were positive for CD2 and CD30 and negative for… read more here.
Keywords: establishment characterization; cell line; chromosome; hlh ... See more keywords
Persistent fever in a pediatric renal transplant patient: Answers
Sign Up to like & getrecommendations! Published in 2018 at "Pediatric Nephrology"
DOI: 10.1007/s00467-018-4130-0
Abstract: Bone marrow biopsy showed presence of intracellular yeast forms along with rare histiocytes showing hemophagocytosis. Histoplasma serum Ag was positive and fungal blood and bone marrow cultures grew H. capsulatum. MRI of the brain with… read more here.
Keywords: cmv; histoplasma serum; bone marrow; therapy ... See more keywords
A Case of Chronic Lymphocytic Leukemia Complicated by Hemophagocytic Lymphohistiocytosis: Identifying the Aberrant Immune Response
Sign Up to like & getrecommendations! Published in 2022 at "Journal of General Internal Medicine"
DOI: 10.1007/s11606-022-07395-7
Abstract: Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome that may complicate hematologic malignancies. HLH and malignancies have common clinical features, and HLH diagnostic criteria (HLH-2004/Hscore) were not validated in this specific population. We describe a… read more here.
Keywords: hlh; chronic lymphocytic; case; hemophagocytic lymphohistiocytosis ... See more keywords
Correspondence to: hemophagocytic lymphohistiocytosis after SARS-CoV-2 vaccination
Sign Up to like & getrecommendations! Published in 2022 at "Infection"
DOI: 10.1007/s15010-022-01820-z
Abstract: We thank Mungmunpuntipantip and colleagues for their interest in our recently published case of a young adult female developing hemophagocytic lymphohistiocytosis (HLH) after BionTech mRNA SARS-CoV-2 vaccine [1]. In their correspondence, the authors ask about… read more here.
Keywords: vaccination; correspondence; hlh; history ... See more keywords
Fatal COVID-19 infections: Is NK cell dysfunction a link with autoimmune HLH?
Sign Up to like & getrecommendations! Published in 2020 at "Autoimmunity Reviews"
DOI: 10.1016/j.autrev.2020.102561
Abstract: Shoenfeld [1] postulates that in COVID-19 infected patients a clinical constellation of cytokine storm, respiratory failure and eventually death is reminiscent of a “hyperferritinemic syndrome” a condition that resembles a hemophagocytic lymphohistiocytosis (HLH)-like syndrome. One… read more here.
Keywords: ivig; infection; covid; cytotoxicity ... See more keywords
Thinking Beyond HLH: Clinical Features of Patients with Concurrent Presentation of Hemophagocytic Lymphohistiocytosis and Thrombotic Microangiopathy
Sign Up to like & getrecommendations! Published in 2020 at "Biology of Blood and Marrow Transplantation"
DOI: 10.1016/j.bbmt.2019.12.080
Abstract: Introduction Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of excessive immune system activation largely driven by high levels of interferon gamma. The clinical HLH presentation can have considerable overlap with other inflammatory conditions. We present a… read more here.
Keywords: presentation; hemophagocytic lymphohistiocytosis; tma; thrombotic microangiopathy ... See more keywords
Hemophagocytic Lymphohistiocytosis, a Rare Presentation in Lupus Nephritis
Sign Up to like & getrecommendations! Published in 2021 at "Kidney International Reports"
DOI: 10.1016/j.ekir.2020.11.036
Abstract: INTRODUCTION H emophagocytic lymphohistiocytosis (HLH) is a rare immune disorder that is life threatening if not promptly diagnosed and treated. Its identification, however, remains a diagnostic challenge for clinicians, given the large overlap in presenting… read more here.
Keywords: lymphohistiocytosis; hemophagocytosis; disease; hemophagocytic lymphohistiocytosis ... See more keywords
Hemophagocytic lymphohistiocytosis: a case series analysis in a pediatric hospital.
Sign Up to like & getrecommendations! Published in 2021 at "Hematology, transfusion and cell therapy"
DOI: 10.1016/j.htct.2021.04.006
Abstract: INTRODUCTION Hemophagocytic lymphohistiocytosis (HLH) is a rare clinical laboratory condition with high mortality rates, resulting from ineffective overactivation of the immune system. Data in the Brazilian literature is scarce, contributing to the challenge in standardizing… read more here.
Keywords: hemophagocytic lymphohistiocytosis; pediatric hospital; hlh; lymphohistiocytosis case ... See more keywords
Adult-onset hemophagocytic lymphohistiocytosis type 2 presenting as a demyelinating disease.
Sign Up to like & getrecommendations! Published in 2018 at "Multiple sclerosis and related disorders"
DOI: 10.1016/j.msard.2018.07.031
Abstract: Familial hemophagocytic lymphohistiocytosis (HLH) is a rare autosomal recessive life-threatening multisystem inflammatory disorder. It is characterized by excessive production of cytokines and uncontrolled activation of lymphocytes and macrophages leading to widespread organ infiltration and tissue… read more here.
Keywords: onset hemophagocytic; adult onset; disease; hemophagocytic lymphohistiocytosis ... See more keywords