Challenges in managing severe homozygous protein c deficiency: a case report

Protein C deficiency is a rare autosomal recessive disorder associated with a high risk of thromboembolic complications. This case report describes the challenges in managing a 23-year-old woman with severe homozygous protein C type 1 deficiency diagnosed since early infancy. Her medical history included misdiagnosed cellulitis, recurrent thrombosis, and permanent vision loss in one eye. The laboratory workup confirmed a diagnosis of severe protein C deficiency. Management involved a combination of fresh frozen plasma (FFP), protein C concentrate, warfarin, and heparin, with ongoing challenges due to recurrent thrombosis and anaphylaxis to FFP. This case highlights the challenges in the diagnosis and management of severe protein C deficiency. Although current treatment options provide partial control, further research is crucial to develop safer and more effective therapies to improve long-term outcomes for affected patients.

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Publication Details

Journal
Blood Coagulation & Fibrinolysis
Published
2024-11-04
DOI
https://doi.org/10.1097/mbc.0000000000001332
Citations
2
Primary Topic
Blood Coagulation and Thrombosis Mechanisms
Type
article
Field-Weighted Citation Impact
0.91
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article

Challenges in managing severe homozygous protein c deficiency: a case report

Eman Almatter, Maha Bourusly, Mona Bourhama, Sondus Alsharidah et al.
2 citations
Blood Coagulation & Fibrinolysis
Blood Coagulation and Thrombosis Mechanisms
0.91
article

Challenges in managing severe homozygous protein c deficiency: a case report

Eman Almatter, Maha Bourusly, Mona Bourhama, Sondus Alsharidah, Mohamad Adel Obaid
article en
2 citations

Abstract

Protein C deficiency is a rare autosomal recessive disorder associated with a high risk of thromboembolic complications. This case report describes the challenges in managing a 23-year-old woman with severe homozygous protein C type 1 deficiency diagnosed since early infancy. Her medical history included misdiagnosed cellulitis, recurrent thrombosis, and permanent vision loss in one eye. The laboratory workup confirmed a diagnosis of severe protein C deficiency. Management involved a combination of fresh frozen plasma (FFP), protein C concentrate, warfarin, and heparin, with ongoing challenges due to recurrent thrombosis and anaphylaxis to FFP. This case highlights the challenges in the diagnosis and management of severe protein C deficiency. Although current treatment options provide partial control, further research is crucial to develop safer and more effective therapies to improve long-term outcomes for affected patients.

Blood Coagulation & FibrinolysisVol. 36(1)
Good health and well-being
Openalex Percentile: Top 22%
Blood Coagulation and Thrombosis Mechanisms
0.91
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Challenges in managing severe homozygous protein c deficiency: a case report — Eman Almatter, Maha Bourusly, et al. · Blood Coagulation & Fibrinolysis (2024) | TGRS Research Map | TGRS