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lymphomatoid papulosis/groznica

Veza se sprema u međuspremnik
ČlanciKlinička ispitivanjaPatenti
3 rezultatima

A case of febrile ulceronecrotic Mucha-Habermann disease with comorbidities.

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Prijava Registriraj se
Febrile ulceronecrotic Mucha-Habermann disease is a very rare and severe variant of pityriasis lichenoides et varioliformis acuta. Adult cases are difficult to diagnose as in the early course they can mimic erythema multiforme or lymphomatoid papulosis. We report a case of a 38-year-old woman who

[Abrupt onset of papulovesicular lesions: diagnostic features and outcome].

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Prijava Registriraj se
BACKGROUND Abrupt onset of papular lesions, with ulcero necrotic evolution could refers to many dermatitis. Febrile ulceronecrotic Mucha-Habermann disease is an unusual severe form of pityriasis lichenoides and varioliform acuta (PLEVA) characterized with ulceronecrotic eruption potentially
BACKGROUND Pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma is the most frequent type of non-Hodgkin's lymphoma (NHL) that primarily involves the lungs. It represents a rare entity accounting for less than 1% of all NHLs and the clinical features have yet to be clearly
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