Your browser doesn't support javascript.
Rare Case of Refractory Hypoxia and Severe Multiorgan Failure from Secondary Lymphohistiocytosis Successfully Bridged to Treatment with Extracorporeal Membrane Oxygenation Support.
Hundal, Jasmin; Bowers, David; Gadela, Naga Vaishnavi; Jaiswal, Abhishek.
  • Hundal J; Department of Internal Medicine, University of Connecticut, Farmington, Connecticut, United States of America.
  • Bowers D; Department of Internal Medicine, University of Connecticut, Farmington, Connecticut, United States of America.
  • Gadela NV; Department of Internal Medicine, University of Connecticut, Farmington, Connecticut, United States of America.
  • Jaiswal A; Department of Cardiology, Hartford Hospital Heart and Vascular Institute, Hartford, Connecticut, United States of America.
Indian J Crit Care Med ; 26(8): 970-973, 2022 Aug.
Article in English | MEDLINE | ID: covidwho-1979534
ABSTRACT

Introduction:

Acute respiratory distress syndrome (ARDS) is an uncommon complication of hemophagocytic lymphohistiocytosis (HLH). Non-specific findings that mimic other diseases make timely diagnosis and treatment challenging. We present a rare case of severe ARDS and multiorgan failure from secondary HLH due to peripheral T-cell lymphoma. Case presentation A middle-aged female presented with dry cough and fever for three days. On presentation, the patient was febrile to 105°F and hypoxic to 88% on room air. Chest X-ray showed bilateral interstitial infiltrates. Laboratory investigations showed lymphopenia and elevated inflammatory markers. The viral panel, including coronavirus disease-2019 (COVID-19), influenza, and respiratory syncytial virus (RSV), was negative. Her respiratory status progressively worsened, requiring invasive mechanical ventilation for ARDS. Despite lung-protective ventilation, prone positioning, and the use of paralytic agents, the patient continued to remain hypoxic, necessitating extracorporeal membrane oxygenation (ECMO) support. The patient was started on antibiotics and high-dose steroid. Thereafter, she developed a leukemoid reaction, and the ferritin level started rising; raising suspicion for lymphophagocytosis. During this time, she also developed acute liver and kidney failure and required multiple vasopressors and renal replacement therapy. Eventually, a diagnosis of mature peripheral T-cell lymphoma was established. Subsequently, her respiratory status and multiorgan failure significantly improved, and ECMO was explanted after 2 weeks. She was started on etoposide and steroid, and eventually discharged after 6 weeks.

Discussion:

This is the first case describing a successful implementation of ECMO in an adult diagnosed with ARDS secondary to mature peripheral T-cell lymphoma; allowing for recovery of respiratory status, which was compromised during the initial cytokine storm and provided time to establish the diagnosis and initiate appropriate treatment of secondary HLH mature due to peripheral T-cell lymphoma, and in the end, prevented a fatality. We believe that ECMO may be appropriately instituted in rapidly deteriorating patients with an unknown illness refractory to conventional therapy, to allow for end-organ recovery, to reach a diagnosis, and to administer appropriate therapy. How to cite this article Hundal J, Bowers D, Gadela NV, Jaiswal A. Rare Case of Refractory Hypoxia and Severe Multiorgan Failure from Secondary Lymphohistiocytosis Successfully Bridged to Treatment with Extracorporeal Membrane Oxygenation Support. Indian J Crit Care Med 2022;26(8)970-973. Statement of Ethics This is a case report and does not contain any images or patient identifying information.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Case report Language: English Journal: Indian J Crit Care Med Year: 2022 Document Type: Article Affiliation country: Jp-journals-10071-24284

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Type of study: Case report Language: English Journal: Indian J Crit Care Med Year: 2022 Document Type: Article Affiliation country: Jp-journals-10071-24284