Indian Pediatrics Case Reports (Jan 2021)

A rare case of factor XIII deficiency presenting with scrotal hematoma in an adolescent

  • Rajesh K Kulkarni,
  • Sagar Vartak,
  • Niharika Karandikar,
  • Aarti Kinikar

DOI
https://doi.org/10.4103/ipcares.ipcares_13_21
Journal volume & issue
Vol. 1, no. 1
pp. 5 – 7

Abstract

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Background: Factor XIII deficiency is a rare disorder that may be congenital or acquired and is considered if a coagulation disorder is suspected, but the initial laboratory investigations are normal. Clinical Description: A 10-year-old boy presented with a scrotal swelling and pain following minor trauma. Local examination showed redness of overlying scrotal skin with tenderness on palpation. Management: Initial laboratory investigations for coagulation (prothrombin time/activated partial thromboplastin time/thrombin time) were normal. The diagnosis of factor XIII deficiency was clinched by abnormal clot solubility test. Child was treated with fresh-frozen plasma. Conclusion: Scrotal hematoma is a rare site for bleeding in factor XIII deficiency, which must be suspected if clinical suspicion of coagulation disorder is high and initial laboratory tests for coagulation are normal.

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