1986
Normolipemic eruptive cutaneous xanthomatosis
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1988
2024
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Cited by 16 publications
(17 citation statements)
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“…Light microscopy provides no data suitable for differential diagnosis in most xanthomatous lesions. In primary non‐X histiocytoses, the ultrastructural findings are also insufficiently characteristic, disclosing intracytoplasmic lysosomes, lipid vacuoles, myelin figures, and crystalline cleftlike spaces 12–14 . Similar ultrastructural results were described by Ferrando and Bombi in two cases of xanthoma disseminatum 10 …”
Section: Discussionsupporting
confidence: 60%
“…Light microscopy provides no data suitable for differential diagnosis in most xanthomatous lesions. In primary non‐X histiocytoses, the ultrastructural findings are also insufficiently characteristic, disclosing intracytoplasmic lysosomes, lipid vacuoles, myelin figures, and crystalline cleftlike spaces 12–14 . Similar ultrastructural results were described by Ferrando and Bombi in two cases of xanthoma disseminatum 10 …”
Section: Discussionsupporting
confidence: 60%
“…Different types of xanthomatous lesions may occur in the same patient (1,2). Our patient is presently diagnosed as having normolipemic papuloeruptive xanthomatosis (6).…”
Section: Discussionmentioning
confidence: 96%
“…The condition needs to be differentiated from other systemic diseases which may present with cutaneous xanthomas. Papulonodular xanthomas are also seen with heterozygous FH and other forms of xanthomas like xanthoma disseminatum and verruciform xanthoma seen to be associated with normolipidaemic patients 10 11. Diffuse normolipidaemic xanthomatosis is characterised by normal lipid levels but may be associated with hepatic dysfunction, multiple myeloma, IgG gammopathy, hypernephroma or even chronic myelomonocytic leukaemia 12–14.…”
Section: Discussionmentioning
confidence: 99%
