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An Interesting Case of Hemophagocytic Lymphohistiocytosis Presenting with Pulmonary Hypertension

2010· article· en· W2556420569 on OpenAlexaff
Lauren Gerard, Katharine He Xing, Christine Cserti‐Gazdewich

Bibliographic record

VenueBlood · 2010
Typearticle
Languageen
FieldMedicine
TopicAutoimmune and Inflammatory Disorders Research
Canadian institutionsUniversity Health NetworkUniversity of Toronto
Fundersnot available
KeywordsMedicineHemophagocytosisHemophagocytic lymphohistiocytosisHepatosplenomegalyCytopeniaInternal medicineImmunologyGastroenterologyPancytopeniaBone marrow

Abstract

fetched live from OpenAlex

Abstract Abstract 4728 Introduction: Adult hemophagocytic lymphohistiocytosis (HLH) is a rare and potentially life-threatening hyperinflammatory syndrome that presents both diagnostic and therapeutic challenges. HLH may be primary and related to an underlying genetic abnormality or secondary to infection, malignancy, or rheumatologic condition. We describe a case of HLH in a latently EBV-/CMV-/HBV-immune 52-year old male presenting with severe pulmonary hypertension. He was intolerant of the HLH 2004 protocol but responded to salvage therapy with anti-CD52 monoclonal therapy (alemtuzumab). Case Presentation: The patient was previously healthy with a diagnosis of axonal-pattern CIDP five years prior. He had a one year history of mild progressive exertional dyspnea and experienced a flu-like illness treated as presumed H1N1 infection five months prior. He presented to hospital with progressive respiratory distress, fevers and weight loss, culminating in respiratory failure requiring mechanical ventilation for 4 days. Investigations revealed severe pulmonary hypertension (RVSP 112 mmHg), nephrotic range proteinuria, transaminitis, hyperferritenemia (ferritin 4240 ug/L) and hepatosplenomegaly. Initial hematologic investigations revealed an isolated thrombocytopenia (IVIG and steroid non-responsive), soon followed by hemolytic anemia with an oxidative blood film. Initial bone marrow biopsy showed normal hematopoiesis, megakaryoyctic thrombocytopenia, iron deficiency, and no evidence of hemophagocytosis. Rheumatologic investigations were negative (ANA, ENA, C3, C4, p-ANCA, c-ANCA, ds-DNA, anti-GBM) and viremia investigations negative (HIV, CMV, EBV, HBV). Hematologic causes of peripherally destructive cytopenias were ruled out (DAT, PNH, methemoglobin, APLA, ADAMTS13, G6PD, PK normal). No definitive etiology of pulmonary hypertension was found and treatment was initiated with nitric oxide and sildenafil. Four weeks after initial presentation to hospital, he developed worsening pancytopenia and unexplained fevers. Repeat bone marrow examination revealed hemophagocytosis, achieving sufficient criteria for diagnosis with HLH. Repeat EBV serology was IgM positive with a viral load 7 × 105/ml. HLH 2004 protocol was initiated, however within 7 days, treatment-limiting nephrotoxicity and hepatotoxicity developed, prompting discontinuation of cyclosporine and dose-reduction of etoposide. Hepatic biopsy revealed drug-induced sinusoidal necrosis with no HLH involvement. Evidence of worsening HLH (ongoing fevers, cachexia, debility, severe cytopenias requiring transfusion and filgrastim support, and increasing ferritin) prompted the use of alemtuzumab. Within 7 days of alemtuzumab initiation the ANC increased from less than 0.2 to within normal range, and within 14 days platelet count rebounded to above 50. Ferritin fell from a peak of 4756 ug/L to approximately 1500 ug/L. Treatment course was complicated by severe upper and lower gastrointestinal bleeds (necessitating massive transfusion protocol), pulmonary blastomycosis (treated with ambisome and itraconazole) and several episodes of bacteremia. Despite his precarious course in hospital, he responded to 6 weeks of treatment with alemtuzumab with continued improvement in his clinical, biochemical, and hematological manifestations of HLH. At 105 days of post-diagnosis follow-up to date, his HLH remains in remission with gradual, ongoing improvement in pulmonary hypertension. Although no clear diagnostic association has been proven, we hypothesized that either this patient's pulmonary hypertension and HLH had a common precipitant or that his pulmonary hypertension was secondary to HLH disease activity. Conclusion: This is a unique case of HLH presenting concurrently with severe pulmonary hypertension, complicated by intolerance of the HLH 2004 protocol, but response to salvage anti-CD52 therapy. There is still much to be understood about the underlying pathophysiology and treatment strategies of HLH. Disclosures: Off Label Use: Alemtuzumab is a monoclonal antibody which targets CD52. It is used as second-line treatment for chronic lymphocytic leukemia. It is also used off-label for other lymphocyte/NK cell disorders, such as cutaneous T-cell lymphoma and some autoimmune diseases. It has been described in off-label use for hemophagocytic lymphohistiocytosis (HLH) as a bridge to allogeneic stem cell transplant.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Case report · Consensus signal: Case report
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.004
Threshold uncertainty score0.012

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.002
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0020.001
Science and technology studies0.0020.001
Scholarly communication0.0020.002
Open science0.0010.001
Research integrity0.0040.003
Insufficient payload (model declined to judge)0.0030.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.020
GPT teacher head0.280
Teacher spread0.260 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designCase report
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2010
Admission routes1
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