Recurrent thrombosis in a young female: unmasking protein S deficiency
Authors:
Vinay Kumar Rastogi
, Paras Passi
, Jithin Jose
, Kishankumar Kotadiya
,
Abstract
Background: Hereditary protein S deficiency is a rare but significant cause of unprovoked, recurrent venous thromboembolism (VTE) in young individuals. Early recognition is essential to prevent recurrence and complications.
Case Presentation: A 23-year-old female with previous episodes of deep vein thrombosis (DVT) in 2022 and 2023 presented with acute dyspnea. Imaging revealed pulmonary thromboembolism with bilateral DVT. Coagulation testing confirmed protein S deficiency. She received systemic thrombolysis with tenecteplase followed by heparin infusion and was later transitioned to longterm direct oral anticoagulants. Cardiac function improved following treatment.
Conclusion: This case highlights the importance of considering hereditary protein S deficiency in young patients with recurrent VTE, where early diagnosis and lifelong anticoagulation can prevent morbidity and improve outcomes.
Keywords: Case report, Protein S deficiency, inherited thrombophilia, Venous thromboembolism(VTE),Deep vein thrombosis(DVT), Pulmonary thromboembolism(PTE), Anticoagulation therapy
Pubmed Style
Vinay Kumar Rastogi, Paras Passi, Jithin Jose, Kishankumar Kotadiya. Recurrent thrombosis in a young female: unmasking protein S deficiency. EJMCR. 2026; 04 (February 2026): 65-66. doi:10.24911/ejmcr.9-2279
Publication History
Received: July 29, 2025
Revised: October 24, 2025
Accepted: November 06, 2025
Published: February 04, 2026
Authors
Vinay Kumar Rastogi
Senior Consultant, Jaipur Golden Hospital, New Delhi, India
Paras Passi
Consultant, internal Medicine, Jaipur Golden Hospital, New Delhi, India
Kishankumar Kotadiya
Senior resident in General Medicine, Jaipur Golden Hospital, New Delhi, India