1. Hematologic complications in vascular malformations: A case study of 2 patients.
- Author
-
Matus, Iwona, Bator, Kaja, Machaj, Weronika, Krzemienowska-Cebulla, Aleksandra, Dorochowicz, Mateusz, Senat, Hanna, Korbecki, Adrian, Szuba, Andrzej, and Rabczyński, Maciej
- Subjects
ARNOLD-Chiari deformity ,THROMBOTIC thrombocytopenic purpura ,FIBRIN fibrinogen degradation products ,DISSEMINATED intravascular coagulation ,HUMAN abnormalities ,AVOIDANCE conditioning ,BLOOD coagulation factors ,FIBRIN - Abstract
We present two cases of patients treated at the Angiology, Arterial Hypertension and Diabetology Clinic of the Wroclaw Medical University (UMW) due to vascular malformations, where LIC (localized intravascular coagulation), DIC (disseminated intravascular coagulation) and KMS (Kasabach-Merritt syndrome) occurred. The first case involves a 14-year-old boy admitted with a diagnosis of vascular malformation of the lower limb established at the age of 3. The patient was admitted for the initiation of Sirolimus therapy. The second patient is a 33-year-old man diagnosed with a malformation of the left lower limb involving the pelvis, abdominal cavity, and chest, currently admitted due to coagulation disorders, complicated by life-threatening Kasabach-Merritt syndrome (KMS). The phenomenon occurred after a limb injury. Vascular malformations are congenital vascular anomalies resulting from a disruption in the vasculogenesis process. (1) They are congenital changes that enlarge as the child develops and do not undergo spontaneous involution. They can be classified based on the type of vessels involved (capillary, arterial, venous, lymphatic, mixed) and the nature of the vascular flow (lowflow and high-flow). The clinical presentation of vascular malformations is highly diverse, and despite being congenital, they can remain asymptomatic for a long time, complicating the diagnostic process. (1,3) The presence of malformations carries the risk of health-threatening complications. One such complication is Kasabach-Merritt syndrome, characterized by thrombocytopenia, microangiopathic hemolytic anemia, and consumptive coagulopathy in the presence of a rapidly enlarging vascular tumor. (4,5) Another threat is a coagulopathy limited to the vascular anomaly (LIC). It is characterized by elevated D-dimers and fibrin degradation products, low levels of fibrinogen, FV, FVIII, FXIII, and antithrombin, and sometimes mild to moderate thrombocytopenia. (6,7) Early implementation of anticoagulant therapy allows for the avoidance of health-threatening conditions and the development of disseminated intravascular coagulation syndrome (DIC). (8). [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF