<scp>LUMBAR</scp> Syndrome State‐Of‐The‐Art Review: Insights Into a Rare and Complex Condition
LUMBAR syndrome is a rare condition with natural history and long-term outcomes that have not been well described. This acronym represents the constellation of features associated with the condition: Lower body hemangiomas with Urogenital anomalies and Ulceration, spinal cord Malformations, Bony defects of the spine and lower extremities, and Anorectal, Arterial, and/or Renal anomalies. The associated infantile hemangioma is the most notable feature, which occurs in a segmental pattern affecting the lower half of the body. Recent publications have described the clinical features of LUMBAR syndrome, its overlap with other lower body syndromes, and, notably, a landmark paper establishing diagnostic criteria through Delphi consensus. This paper aims to provide a comprehensive review of the clinical features, diagnostic criteria, pathophysiology, treatment options, and outcomes associated with LUMBAR syndrome.
Authors
- Dawn H. Siegel (ORCID: https://orcid.org/0000-0001-6546-2693)
- Denise W. Metry (ORCID: https://orcid.org/0000-0003-1991-1683)
- Jordan Bui (ORCID: https://orcid.org/0000-0003-1575-7156)
- Bianca Martin (ORCID: https://orcid.org/0000-0003-1686-6186)
- Alleana Corpin
Institutions
- Georgetown University (US)
- Driscoll Children's Hospital (US)
- University of Missouri–Kansas City (US)
- Stanford University (US)
Publication Details
- Journal
- Pediatric Dermatology
- Published
- 2025-09-18
- DOI
- https://doi.org/10.1111/pde.70024
- Primary Topic
- Vascular Malformations and Hemangiomas
- Type
- article
- Field-Weighted Citation Impact
- 0.00