
pmid: 40693676
Abstract Haemophagocytic lymphohistiocytosis (HLH) is a rare complication of rickettsial infections. We report a 50-y-old man from northern India who presented with fever, respiratory distress, altered sensorium and an eschar. Despite treatment with doxycycline, his condition deteriorated with multi-organ dysfunction. PCR and sequencing from the eschar confirmed Rickettsia conorii. Bone marrow examination, elevated ferritin and triglycerides, as well as an H-score of 224 confirmed HLH. The patient was treated with corticosteroids but succumbed to refractory ventricular arrhythmias. A high index of suspicion is essential in rickettsial infections that present with multi-organ dysfunction, as early recognition of HLH enables the prompt initiation of treatment of the underlying disease and adjunctive immunosuppressive therapy. [GenBank accession nos. U59728.1 and MZ779037.]
Male, Rickettsia conorii, Fatal Outcome, Doxycycline, Humans, Middle Aged, Boutonneuse Fever, Polymerase Chain Reaction, Lymphohistiocytosis, Hemophagocytic, Anti-Bacterial Agents
Male, Rickettsia conorii, Fatal Outcome, Doxycycline, Humans, Middle Aged, Boutonneuse Fever, Polymerase Chain Reaction, Lymphohistiocytosis, Hemophagocytic, Anti-Bacterial Agents
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