A patient with Baller–Gerold syndrome and midline NK/T lymphoma
✍ Scribed by Marusa Debeljak; Aleksandra Zver; Janez Jazbec
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 373 KB
- Volume
- 149A
- Category
- Article
- ISSN
- 1552-4825
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📜 SIMILAR VOLUMES
The term Baller-Gerold syndrome was coined by Cohen [1979: Birth Defects 15(5B): 13-63] to designate the phenotype of craniosynostosis and radial aplasia. It is thought to be a rare autosomal recessive condition, which, in some patients, presents with additional abnormalities, such as polymicrogyria
We present a case of a patient who developed all manifestations of thrombotic thrombocytopenic purpura-hemolytic uremic syndrome (TTP-HUS) acutely following treatment of cutaneous T-cell lymphoma (CTCL, Sezary syndrome) with deoxycoformycin (pentostatin). Symptoms and signs included severe thrombocy