2021
DOI: 10.1186/s13256-021-02900-8
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Ganglionar tuberculosis infection evolving to hemophagocytic lymphohistiocytosis after anti-programmed cell death 1 treatment for high-risk melanoma: a case report

Abstract: Background Hemophagocytic lymphohistiocytosis is a rare, potentially fatal syndrome of immune hyperactivation. Here we describe a ganglionar tuberculosis evolving to hemophagocytic lymphohistiocytosis following adjuvant immunotherapy in a melanoma patient. Case presentation A 76-year-old Caucasian male with melanoma started with fever, diffuse petechiae, splenomegaly, anemia, thrombocytopenia, hypofibrinogenemia, and hyperferritinemia 2 months foll… Show more

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Cited by 3 publications
(1 citation statement)
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“…) Resolution AIHA, auto-immune hemolytic anemia; CLL, chronic lymphocytic leukemia; Dab/Tram, dabrafenib/trametinib; DAT, direct antigen test; HLH, hemophagocytic lymphohistiocytosis; ICI, immune checkpoint inhibitor; Ipi, ipilimumab; irAE, immune-related adverse event; MM, mycophenolate mofetil; Nivo, nivolumab; Pembro, pembrolizumab[17][18][19][20][21][22][23][24][25][26][27][28][29][30].…”
mentioning
confidence: 99%
“…) Resolution AIHA, auto-immune hemolytic anemia; CLL, chronic lymphocytic leukemia; Dab/Tram, dabrafenib/trametinib; DAT, direct antigen test; HLH, hemophagocytic lymphohistiocytosis; ICI, immune checkpoint inhibitor; Ipi, ipilimumab; irAE, immune-related adverse event; MM, mycophenolate mofetil; Nivo, nivolumab; Pembro, pembrolizumab[17][18][19][20][21][22][23][24][25][26][27][28][29][30].…”
mentioning
confidence: 99%