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Severe Mucha-Habermann-Like Ulceronecrotic Skin Disease in T-Cell Acute Lymphoblastic Leukemia Responsive to Basiliximab and Stem Cell Transplant.

Abstract
A 5-year-old girl with T-cell acute lymphoblastic leukemia (T-ALL) developed a progressive eruption of crusted papules and ulcerative plaques involving 80% of her body surface area with histopathology consistent with febrile ulceronecrotic Mucha-Habermann disease (FUMHD), although multiple specimens also contained clonal leukemic cells. Her skin disease was refractory to many classic treatments for FUMHD, including methotrexate, and became so severe that concern about superinfection prevented intensification of chemotherapy for her malignancy. The addition of basiliximab promoted gradual improvement of the skin, allowing for chemotherapy intensification and subsequent bone marrow transplantation, after which the eruption resolved completely. This report describes a severe case of FUMHD-like eruption associated with clonal leukemic cells that improved with basiliximab, suggesting anti-CD25 therapy as a novel treatment for ulceronecrotic skin disease in the setting of high interleukin-2 levels.
AuthorsLauren A V Orenstein, Carrie C Coughlin, Andrea T Flynn, Vinodh Pillai, Markus D Boos, Gerald B Wertheim, James R Treat, David T Teachey
JournalPediatric dermatology (Pediatr Dermatol) Vol. 34 Issue 5 Pg. e265-e270 (Sep 2017) ISSN: 1525-1470 [Electronic] United States
PMID28884915 (Publication Type: Case Reports, Journal Article)
Copyright© 2017 Wiley Periodicals, Inc.
Chemical References
  • Antibodies, Monoclonal
  • Immunosuppressive Agents
  • Recombinant Fusion Proteins
  • Basiliximab
Topics
  • Antibodies, Monoclonal (therapeutic use)
  • Antineoplastic Combined Chemotherapy Protocols
  • Basiliximab
  • Child, Preschool
  • Female
  • Herpes Simplex (complications, therapy)
  • Humans
  • Immunosuppressive Agents (therapeutic use)
  • Pityriasis Lichenoides (complications, therapy)
  • Precursor T-Cell Lymphoblastic Leukemia-Lymphoma (complications, therapy)
  • Recombinant Fusion Proteins (therapeutic use)
  • Skin (pathology)
  • Stem Cell Transplantation (methods)

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