key: cord-1033637-l6tt7pky authors: Jariwal, Roopam; Jaber, Fouad S.; Ipalawatte, Harendra; Petersen, Greti title: An Unusual Case of Hemophagocytic Lymphohistiocytosis Presentation in Acute Human Immunodeficiency Virus date: 2021-06-02 journal: J Investig Med High Impact Case Rep DOI: 10.1177/23247096211021696 sha: 4d081954b63b42866eb0c544fb73879e8e0d920f doc_id: 1033637 cord_uid: l6tt7pky Hemophagocytic lymphohistiocytosis (HLH) in acute human immunodeficiency virus (HIV) patients has been scarcely reported in the English literature. To the best of our knowledge, only 12 cases have been described. We present a case of a 27-year-old male with no past medical history who was admitted with a new-onset headache, fever, night sweats, and chills. Further laboratory tests revealed transaminitis, leukopenia, thrombocytopenia, positive HIV antigen/antibody test, and markedly elevated ferritin levels, which promoted our suspicion of HLH. This case demonstrates HLH as an unusual presentation of HIV during its seroconversion stage. This report adds a rare disease process to the available literature, and we emphasize that markedly elevated ferritin levels in acute HIV patients should raise suspicion toward a diagnosis of HLH. Hemophagocytic lymphohistiocytosis (HLH) is a rare but potentially life-threatening condition marked by immune dysregulation resulting in cytokine storm, abnormal function of T lymphocytes, with activation of macrophages leading to hemophagocytes in the reticuloendothelial system. [1] [2] [3] HLH has been reported at all stages of HIV infection. 4 In the majority of cases, AIDS is the main underlying etiology during which opportunistic infections trigger the onset of HLH. However, HIV itself has been reported as the cause of HLH. In this report, we highlight HIV as a triggering agent of HLH and propose antiretroviral therapy (ART) as a viable option in managing acute HIV-HLH. We emphasize hyperferritinemia as an important clue toward the diagnosis of HLH. A 27-year-old male with no past medical history presented to the emergency department with headache for the past 2 days. He also endorsed photophobia, chills, night sweats, decreased appetite, 10-pound unintentional weight loss, and fevers. The patient reported being sexually active with men only with the last unprotected sexual intercourse 2 weeks ago. He denied any illicit drug use. In the emergency department, the patient had a temperature of 38.2 °C, a heart rate of 103 beats/minutes, respiratory rate of 20 breaths/minutes, blood pressure of 100/60 mm Hg, and O 2 saturation of 100% on room air. Physical examination was unremarkable with no meningeal signs. Given his headache and a fever of 38.3 °C, the patient was started on empiric meningitis treatment with vancomycin and ceftriaxone. Computed tomography of the head without contrast showed no acute intracranial process. Magnetic resonance imaging of the brain with and without contrast was unremarkable. Initial laboratory findings (Table 1) were significant for leukopenia of 2.2 × 10 3 /µL, thrombocytopenia of 81 × 10 3 /µL, hemoglobin of 12.3 g/dL, transaminitis, elevated C-reactive protein of 3.16 mg/dL, and hypoalbuminemia. Chest X-ray did not reveal any active infection or any other pathology. Blood cultures were negative. Lumbar puncture revealed the following: white blood cells 3 cells/ cm 2 , red blood cells 378 cells/cm 2 , glucose 54 mg/dL, and elevated protein 51 mg/dL. Cerebrospinal fluid (CSF) was negative for cryptococcal antigen, herpes simplex virus, and CSF VDRL. Accordingly, vancomycin was discontinued. Ceftriaxone was decreased to 1 g every 24 hours for 2 weeks, followed by intramuscular benzathine penicillin G 3 million units to treat presumed neurosyphilis due to elevated protein in the CSF. HIV antigen/antibody test was positive, with an HIV-RNA level over 10 000 000 copies/ mL, CD4 T-cell count of 201 cells/µL, and CD8 T-cell count of 93 cells/µL. These results along with fatigue, fever, pancytopenia, and transaminitis supported the diagnosis of acute retroviral syndrome; therefore, ART was initiated consisting of darunavir/cobicistat/emtricitabine/ tenofovir alafenamide. Additional laboratory values (Tables 1 and 2) showed hyperferritinemia >40 000 ng/mL, D-dimer >5000 ng/dL, bi-cytopenia, transaminitis, and hypertriglyceridemia, which raised concern for HLH. H-score showed a 93% to 96% probability of having HLH (Table 3) . A collaborative decision was made by the patient and the physicians to defer bone marrow biopsy and we chose to confirm our suspicion by performing noninvasive tests such as interleukin (IL)-2 receptor and natural killer (NK) cell activity. Computed tomography of the abdomen and pelvis with contrast showed borderline prominent right hepatic lobe, slight hypodensity of the liver suggesting fatty hepatocellular changes, and mesenteric adenitis. The patient's symptoms of headache had self-resolved on the third day of admission and he left against medical advice. Following discharge, IL-2R returned >4000 pg/mL. The suspicion of HLH secondary to acute HIV was confirmed as the patient met 4/8 criteria for the diagnosis including fever, bi-cytopenia of thrombocytopenia and neutropenia, elevated ferritin, elevated IL-2R along with the high probability of H-score. The patient followed-up outpatient and he reported complete resolution of his symptoms. Hemophagocytic lymphohistiocytosis was first described by Scott and Robb-Smith in 1939. 5 Primary or genetic HLH occurs in infants and young children due to mutations in genes responsible for the cytotoxic function of NK cells and T lymphocytes. Secondary HLH occurs in adults, and it is often secondary to infections, malignancies, autoimmune conditions, and acquired immunodeficiency states like HIV/ AIDS. 6 Among infections, viruses are the most common triggering agents (especially Epstein-Barr virus and cytomegalovirus), followed by bacteria (particularly mycobacterium tuberculosis), protozoa (mainly Leishmania spp), and fungi (typically Histoplasma spp). 7-10 The most frequent malignancies associated with HLH are lymphoma, and related autoimmune diseases such as systemic lupus erythematosus and adults Still's disease. 11 The diagnosis of HLH was based on the HLH-2004 criteria proposed by the Histiocyte Society. This HLH-2004 criteria requires 5 out of 8 criteria to make the diagnosis: 12 Our patient achieved 4 out of 8 HLH-2004 criteria (fever, marked elevated ferritin, bi-cytopenia, and high levels of IL-2) and he had an H-score of 211 with a 93% to 96% probability of having HLH. The ideal diagnosis of HLH requires biopsy with histopathological documentation of hemophagocytosis in bone marrow biopsy showing activated histiocytes. But bone marrow biopsy results may also be inconclusive as these findings may be absent in a significant portion of patients, even during fulminant disease. Acute HIV is usually known to have high levels of viremia that is associated with alteration of cytokine levels. 13 The presence of viremia and the subsequent changes of cytokine levels may be associated with the HLH occurrence. HLH is rare in HIV patients with most cases described in chronic HIV or with the presence of opportunistic infections. Only 14 case reports described HLH in HIV acute retroviral syndrome in the English literature [14] [15] [16] [17] [18] [19] [20] [21] [22] (Table 4 ). Our case further confirms that HLH can occur during the seroconversion stage of acute HIV infection. In our case, the markedly elevated ferritin levels, along with thrombocytopenia and transaminitis in this patient with newly diagnosed HIV raised our suspicion toward HLH. Even though the elevation of serum ferritin may occur in acute inflammatory syndrome due to infectious, neoplastic, autoimmune, and iron overload such as hemochromatosis, a cutoff of >10 000 increases the specificity of HLH. 23 To identify the triggering agents of HLH in our patient, we performed numerous imaging studies along with various cultures and serological markers for a number of pathogens and rheumatological and immunological markers. Despite the extensive workup, we were unable to find another triggering agent for HLH except for the HIV infection itself. Subsequently, the most likely explanation is that HLH was a manifestation of the inflammatory storm occurring during acute HIV infection. HLH in acute HIV patients is thought to have a better prognosis compared with HLH due to malignancy. 24 Another difference is that HLH in HIV patients has good prognosis with initiation of ART. Admittedly, all the reported 12 cases attained complete resolution from HLH after the introduction of ART or supportive therapy like steroids or intra venous immunoglobulin. Of 12 cases, 7 cases included the administration of ART during acute HIV infection (Table 4 ). Just like in our case, where the patient had complete resolution of symptoms with ART therapy. Acute HIV infection should be included in the differential diagnosis of HLH. Since our patient recovered with ART without the need for any further intervention, screening for HIV should be performed as it can affect the patient's outcome significantly. A missed diagnosis of HIV in young adults who are diagnosed with HLH may lead to exposure to immune-modulating therapy that comes with their own side effects. We emphasize that histopathological presence of hemophagocytosis is not a prerequisite to making a clinical diagnosis of HLH. We further stress the importance of hyperferritinemia as an important clue toward the diagnosis of HLH in HIV patients. HLH-2004: diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis Hemophagocytic lymphohistiocytosis: an update on diagnosis and pathogenesis Familial and acquired hemophagocytic lymphohistiocytosis Haemophagocytic syndrome and HIV Histiocytic medullary reticulosis The challenging diagnosis of haemophagocytic lymphohistiocytosis in an HIVinfected patient Adult haemophagocytic syndrome Hemophagocytic lymphohistiocytosis associated with viral infections: diagnostic challenges and therapeutic dilemmas Infections associated with haemophagocytic syndrome Secondary hemophagocytic lymphohistiocytosis in zoonoses. 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The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. The author(s) received no financial support for the research, authorship, and/or publication of this article. Ethical approval to report this case was obtained from the Kern Medical Institutional Review Board (Study ID #20088). Informed consent for patient information to be published in this article was obtained. Roopam Jariwal https://orcid.org/0000-0002-2506-476X