Literature DB >> 33563711

Purpura fulminans as the presenting manifestation of COVID-19.

Ismat Ara Khan1, Supratim Karmakar1, Uddalak Chakraborty2, Abheek Sil3, Atanu Chandra4.   

Abstract

Entities:  

Keywords:  dermatology; infectious diseases

Year:  2021        PMID: 33563711      PMCID: PMC7878050          DOI: 10.1136/postgradmedj-2020-139202

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN: 0032-5473            Impact factor:   2.401


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A 48-year-old woman presented to our facility with a 2-day history of fever and rapidly enlarging skin discolouration over her right hand. On admission, normal vital parameters were noted. Cutaneous examination revealed two tender necrotic indurated plaques (5×4 cm and 10×6 cm) with focal haemorrhagic bulla and peripheral retiform purpura (figure 1). No abnormality was detected on systemic examination. Reverse transcriptase PCR for SARS-CoV-2 from oropharyngeal and nasopharyngeal swab was positive. Laboratory investigations documented thrombocytopenia (90×109/L), elevated prothrombin time (17.6 s), prolonged activated partial thromboplastin time (53.5 s) along with elevated fibrin degradation products (37 mg/L; normal <10 mg/L) and D-dimer levels (7680 ng/mL; normal <500 ng/mL). Blood culture showed no growth. She was diagnosed with acute infectious (SARS-CoV-2) purpura fulminans and promptly started on anticoagulation therapy. Despite an initial improvement, the patient’s course of illness was complicated with severe acute respiratory distress syndrome and she died after 12 days of hospitalisation.
Figure 1

Multiple erythematous indurated plaques with focal necrosis, haemorrhagic bullae and peripheral retiform purpura.

Multiple erythematous indurated plaques with focal necrosis, haemorrhagic bullae and peripheral retiform purpura. COVID-19 has been declared a pandemic by the WHO and has claimed innumerable lives until today. Though, majority of the cases present with respiratory symptoms, coagulation abnormalities and thrombosis in severe SARS-CoV-2 infection and its cutaneous manifestations are being increasingly recognised.1 Recently, livedoid and necrotic eruptions were noted in patients with more severe occlusive vascular disease.2 Purpura fulminans (PF) is a life-threatening disorder characterised by rapidly progressive cutaneous haemorrhage and necrosis caused by vascular thrombosis and disseminated intravascular coagulation. Three distinct categories identified include neonatal (inherited or acquired abnormalities of protein C, S or other coagulation systems), acute infectious (meningococcus, Gram-negative bacilli, Staphylococcus and varicella) and idiopathic.3 4 Physicians caring for patients with COVID-19 should recognise PF as a potential manifestation of underlying coagulopathy and immediately initiate anticoagulation therapy.
  4 in total

Review 1.  COVID-19 Sepsis: Pathogenesis and Endothelial Molecular Mechanisms Based on "Two-Path Unifying Theory" of Hemostasis and Endotheliopathy-Associated Vascular Microthrombotic Disease, and Proposed Therapeutic Approach with Antimicrothrombotic Therapy.

Authors:  Jae C Chang
Journal:  Vasc Health Risk Manag       Date:  2021-06-01

Review 2.  COVID-19 associated symmetrical peripheral gangrene: A case series.

Authors:  Abheek Sil; Uddalak Chakraborty; Atanu Chandra; Surajit Kumar Biswas
Journal:  Diabetes Metab Syndr       Date:  2021-11-27

3.  Severe Acute Respiratory Syndrome Coronavirus-2 Pneumonia Presenting Concomitantly With Purpura Fulminans: A Case Report.

Authors:  Giulio Ciprian
Journal:  Cureus       Date:  2022-01-13

4.  COVID-19 association with purpura fulminans: report of a life threatening complication in a fully vaccinated patient.

Authors:  Vladislav Pavlovich Zhitny; Mitchell Lyons; Andrea Perloff; John Menezes; Ashley Pistorio; Richard Baynosa
Journal:  J Surg Case Rep       Date:  2022-03-26
  4 in total

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