Severe Fatal ARDS Due to Untreated Human Granulocytic Anaplasmosis in a 67-Year-Old Man: A Case Report.


Journal

The American journal of case reports
ISSN: 1941-5923
Titre abrégé: Am J Case Rep
Pays: United States
ID NLM: 101489566

Informations de publication

Date de publication:
15 Jul 2024
Historique:
medline: 15 7 2024
pubmed: 15 7 2024
entrez: 15 7 2024
Statut: epublish

Résumé

BACKGROUND Anaplasmosis, or human granulocytic anaplasmosis (HGA), is a tick-borne diseased caused by a gram-negative, intracellular bacterium, Anaplasma phagocytophilum. HGA usually presents with mild symptoms but can be more severe. This report describes a 67-year-old male resident of rural Pennsylvania, admitted to the hospital after a fall, who developed fatal acute respiratory distress syndrome (ARDS) associated with human granulocytic anaplasmosis (HGA) following transmission of Anaplasma phagocytophilum by a tick bite (Ixodes scapularis). CASE REPORT A 67-year-old man, resident of rural Pennsylvania, with history of diabetes mellitus, presented after falling from a 7-foot-tall ladder, sustaining right-sided hemopneumothorax, multiple right rib fractures, and unstable T12 vertebra fracture. He required tube thoracostomy and underwent T9-L2 posterior spinal fusion surgery. His initial labs showed leukopenia, thrombocytopenia, and elevated transaminase levels. His course was complicated by cardiac arrest and acute respiratory failure, consistent with severe ARDS. He received high positive end-expiratory pressure (PEEP) ventilation, prone positioning, and neuromuscular paralysis to improve refractory hypoxemia. Bronchoalveolar lavage (BAL) for bacterial, fungal, viral pathogens, Covid-19, respiratory viral panel, Mycoplasma pneumoniae, and Chlamydia pneumoniae were negative. his family withdrew medical care, knowing the patient's own wishes, and the patient died. Polymerase chain reaction (PCR) for Anaplasma DNA came back positive after the patient's death. His peripheral smear was then examined, showing morulae inside the cytoplasm of infected neutrophils.   CONCLUSIONS This report describes the atypical presentation of a case of HGA and highlights that in parts of the world where tick-borne diseases are endemic, disease awareness, high index of clinical suspicion, and early diagnosis and management are required.

Identifiants

pubmed: 39004878
pii: 943966
doi: 10.12659/AJCR.943966
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e943966

Auteurs

Shehryar Malik (S)

Department of Internal Medicine, University of Pittsburgh Medical Center Mercy Hospital, Pittsburgh, PA, USA.

Martha F Brucato (MF)

Department of Critical Care Medicine, University of Pittsburgh Medical Center Mercy Hospital, Pittsburgh, PA, USA.

Laura Faiver (L)

Department of Critical Care Medicine, University of Pittsburgh Medical Center Mercy Hospital, Pittsburgh, PA, USA.

Tung Phan (T)

Division of Clinical Microbiology, Department of Pathology, University of Pittsburgh Medical Center Mercy Hospital, Pittsburgh, PA, USA.

Mohamed H Yassin (MH)

Division of Infectious Diseases, University of Pittsburgh Medical Center Mercy Hospital, Pittsburgh, PA, USA.

Jonathan M Bishop (JM)

Department of Critical Care Medicine, University of Pittsburgh Medical Center Mercy Hospital, Pittsburgh, PA, USA.

Sumit Kapoor (S)

Department of Critical Care Medicine, University of Pittsburgh Medical Center Mercy Hospital, Pittsburgh, PA, USA.

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