Results 51 to 60 of about 6,887 (246)
Successful Treatment of Paediatric Necrobiosis Lipoidica With Baricitinib
JEADV Clinical Practice, EarlyView.ABSTRACT Necrobiosis lipoidica (NL) is a rare, chronic granulomatous condition that typically presents as sharply demarcated plaques with telangiectasia and atrophic centres. Paediatric cases are uncommon, and treatment options often fail to address refractory cases.
P. Simões Farinha, M. J. Paiva‐Lopes
wiley +1 more source
An exuberant case of necrobiotic xanthogranuloma
Indian Dermatology Online Journal, 2020 Necrobiotic xanthogranuloma (NXG) is a rare form of inflammatory granulomatous disease of the skin characterized by the presence of pruritic to painful lesions, generally located in the periorbital area, although trunk and proximal extremities may also ...
Sofia Lopes +5 more
doaj +1 more source
Necrobiotic xanthogranuloma successfully treated with autologous stem cell transplantation [PDF]
, 2018 Paraproteinemia can be complicated by necrobiotic xanthogranuloma. Therapeutic options for this progressive disease are limited, and there is no agreement on a single best strategy.
Dispenzieri, Angela +7 more
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Clinical Medicine Insights: Case Reports, 2012 Introduction Orbital masses in adults are often caused by systemic diseases or are associated with systemic manifestations. Juvenile xanthogranuloma as a cause is rare and unreported in Africa.
Okosa Michael Chuka +1 more
doaj +1 more source
Cutaneous necrobiotic xanthogranuloma (NXG)--successfully treated with low dose chlorambucil. [PDF]
, 2001 Eur J Dermatol. 2001 Sep-Oct;11(5):458-62. Cutaneous necrobiotic xanthogranuloma (NXG)--successfully treated with low dose chlorambucil. Machado S, Alves R, Lima M, Leal I, Massa A.
Alves, R. +4 more
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Uncommon hepatic tumors: iconographic essay – Part 2 [PDF]
, 2014 In cases where typical aspects are shown, the diagnosis of most frequent hepatic lesions can be made with some safety by means of several imaging methods; on the other hand, uncommon lesions generally represent a diagnostic challenge for the radiologist.
Bormann, Renata Lilian +5 more
core +3 more sources
Necrobiotic Xanthogranuloma [PDF]
Mayo Clinic Proceedings, 2021 Andrew J. Portuguese +2 more
openaire +2 more sources
JEADV Clinical Practice, EarlyView.ABSTRACT Multiple myeloma (MM) is a malignant plasma cell disorder that primarily presents with CRAB symptoms (calcium elevation, renal failure, anemia, and bone abnormalities). In rare cases, MM manifests with systemic complications like skin ulcers, which present management challenges. Here, we report a 78‐year‐old Japanese man with MM and refractory
Naoko Hattori +5 more
wiley +1 more source
Xanthogranulomatous hypophysitis: A rare presentation in a young female patient
Clinical Case Reports, 2022 Hypophysitis is a rare inflammatory condition that may present both clinically and radiologically as a neoplastic lesion. Xanthogranulomas are rare intracranial lesions with controversial etiology.
Mohammad Ali Yaghoubi +4 more
doaj +1 more source
Upper eyelid juvenile xanthogranuloma: a case report
Revista Brasileira de Oftalmologia, 2021 Juvenile xanthogranuloma is a rare benign non-Langerhans cell histiocytosis. Clinical manifestation usually occurs up to the age of 2 years, with yellowish papules and variable clinical progression.
Pedro Henrique Oliveira Ribeiro +4 more
doaj +1 more source