Please use this identifier to cite or link to this item: http://20.193.157.4:9595/xmlui/handle/123456789/5466
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dc.contributor.authorM. S. Kotennavar, Aravind V. Patil-
dc.contributor.authorPradeep Jaju, Narendra Ballal-
dc.date.accessioned2024-03-08T07:19:15Z-
dc.date.available2024-03-08T07:19:15Z-
dc.date.issued2024-
dc.identifier.issn09722068-
dc.identifier.urihttp://20.193.157.4:9595/xmlui/handle/123456789/5466-
dc.description.abstractNicolau syndrome (embolia cutis medicamentosa) is a condition where we see variable degrees of tissue necrosis including the skin and deeper tissues, due to an iatrogenic cause, intramuscular, subcutaneous, intra-articular injections, could be some of them. It occurs due to intravascular inoculation leading to crystal embolization causing thrombotic occlusion, vasospasm, and marked inflammation and surrounding necrosis. Here, we present a case of a 35-year-old gentleman who presented to us with bluish-purple discoloration of the skin followed by a necrotic patch and ulceration with multiple hyperpigmented spots over the back and lower limb post intramuscular diclofenac sodium injection. Routine investigation showed neutrophilia and thrombocytosis with increased creatinine. A diagnosis of Nicolau’s syndrome (embolia cutis medicamentosa) was made clinically, which was confirmed by histopathology following biopsy. Adequate surgical debridement and a combination therapy of analgesics, intravenous antibiotics, intravenous anticoagulants, and vasoactive therapy were administered. Split thickness skin grafting was done once the wound was healthy with rich granulation tissue, after 4 weeks of index surgery in this case. Patient recovered uneventfully.en_US
dc.language.isoenen_US
dc.publisherIndian Journal of Surgeryen_US
dc.subjectEmbolia Cutis Medicamentosaen_US
dc.subjectNicolau’s Syndromeen_US
dc.subjectNecrotizing fasciitisen_US
dc.subjectIntramuscular injectionsen_US
dc.titleA Rare Case of Nicolau’s Syndrome (Embolia Cutis Medicamentosa) Following Intramuscular Diclofenac Sodium Injection in a Young Adulten_US
dc.typeOtheren_US
Appears in Collections:BMJ Case Reports



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