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The complex movement disorder of Kasabach–Merritt syndrome associated with a basal ganglia lesion

✍ Scribed by Christos Ganos; Simone Zittel; Christian Gerloff; Alexander Münchau; Tobias Bäumer


Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
748 KB
Volume
27
Category
Article
ISSN
0885-3185

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✦ Synopsis


Kasabach-Merritt syndrome (KMS) is a severe vascular growth disorder associated with generalized kaposiform hemangioendotheliomas, tufted angiomas, consumptive coagulopathy, and thrombocytopenia. [1][2][3] Since the initial report, 1 case series have addressed its complex pathophysiology and treatment. [2][3][4] The limbs and the torso are commonly affected, followed by the retroperitoneum and the mediastinum. Involvement of the head and neck is very unusual. [2][3][4] There have been no reports of KMS patients with movement disorders.