2017
DOI: 10.1111/ijd.13637
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The clinical spectrum of xanthomatous lesions of the eyelids

Abstract: Yellowish papules, nodules, or plaques, namely "xanthomatous" lesions, may be seen on the eyelids in the course of various disorders. The prototype is "xanthelasma palpebrarum" (XP) that is localized only to the eyelids and may be associated with hyperlipidemia. On the other hand, different types of normolipemic disorders may also cause xanthomatous eyelid lesions. Among these, Langerhans cell histiocytosis, diffuse normolipemic xanthoma, and non-Langerhans cell histiocytoses (papular xanthoma, juvenile xantho… Show more

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Cited by 20 publications
(16 citation statements)
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“…It may represent as a localized idiopathic cutaneous phenomenon or maybe a sign of systemic hyperlipidemia and thus knowing the lipid profile of the patient is important to exclude systemic disease. 10 A miscellaneous group which may show rarely granulomatous lesion like perforating folliculitis was found in three cases which showed dilated infundibulum filled with keratin along with foreign body granuloma.…”
Section: Discussionmentioning
confidence: 95%
“…It may represent as a localized idiopathic cutaneous phenomenon or maybe a sign of systemic hyperlipidemia and thus knowing the lipid profile of the patient is important to exclude systemic disease. 10 A miscellaneous group which may show rarely granulomatous lesion like perforating folliculitis was found in three cases which showed dilated infundibulum filled with keratin along with foreign body granuloma.…”
Section: Discussionmentioning
confidence: 95%
“…6 Periorbital XGN lesions should be distinguished from other adult orbital xanthogranulomatous diseases, as Edheim-Chester disease, adult orbital xanthogranulomatous disease, and adult-onset asthma associated with periocular xanthogranuloma. 7…”
Section: Discussionmentioning
confidence: 99%
“…This raises a residual doubt as to whether the eyelid lesions were actually juvenile xanthogranulomas, which have a reputation for an association with neurofibromatosis and leukemia along with other neoplasms [3]. A report of bilateral, multifocal, bulky tumors [40] raises the question of whether another histiocytic disease may have been responsible, such as Rosai-Dorfman sinus histiocytosis, Erdheim-Chester disease, reticulohistiocytomas, or adult-onset asthma with orbital xanthogranulomas [41-44]. …”
Section: Discussionmentioning
confidence: 99%