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https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4695| Title: | Subcutaneous panniculitis-like T-Cell lymphoma in a child presenting as an abdominal wall mass | Authors: | Kimble, R. Whyte, M. Bairagi, A. |
Issue Date: | 2020 | Source: | 60 , 2020 | Journal: | Journal of Pediatric Surgery Case Reports | Abstract: | Childhood panniculitides are not common. Histopathological diagnostic approach is vital to differentiate this group of pathologies that commonly present with inflammation of the subcutaneous adipose tissue. Pediatric subcutaneous panniculitis-like T-cell lymphomas are rare. Treatment modalities include observation, surgical excision, radiotherapy, immunosuppression, and chemotherapy. The case of an 18-month female who presented with a flank mass that was diagnosed as a subcutaneous panniculitis-like T-cell lymphoma and successfully managed with intensity-reduced, dual agent immunosuppression is described.L20071294932020-07-28 | DOI: | 10.1016/j.epsc.2020.101556 | Resources: | https://www.embase.com/search/results?subaction=viewrecord&id=L2007129493&from=exporthttp://dx.doi.org/10.1016/j.epsc.2020.101556 | | Keywords: | case report;child;clinical article;congenital blood vessel malformation;differential diagnosis;drug tolerability;echography;fat necrosis;female;hematoma;histopathology;human;human tissue;abdominal wall;immunosuppressive treatment;petechia;positron emission tomography;preschool child;priority journal;rare disease;subcutaneous fat;subcutaneous T cell lymphoma;abdominal mass;cyclosporineprednisolone;immunohistochemistry;article;bone marrow biopsy;cancer chemotherapy;cancer regression;cancer surgery | Type: | Article |
| Appears in Sites: | Children's Health Queensland Publications |
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