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1.
Actas Dermosifiliogr ; 99(1): 61-3, 2008.
Article in Spanish | MEDLINE | ID: mdl-18206088

ABSTRACT

Neutrophilic dermatoses constitute a clinically heterogeneous group of diseases that share a common histological substrate, consisting of a dense dermal inflammatory infiltrate of mature polymorphonuclear neutrophils and no evidence of vasculitis. We describe the case of a 56-year-old man with a 6-month history of painful generalized erythematous edematous plaques. Histopathology indicated neutrophilic dermatosis but the patient did not have fever, elevated white blood cell count, or systemic involvement. Tests to rule out possible inflammatory, neoplastic, or infectious processes were negative. We consider the term chronic recurrent annular neutrophilic dermatosis, first used by Christensen et al, to be the most appropriate to define this variant with clinical findings that differ from classic Sweet syndrome.


Subject(s)
Sweet Syndrome/classification , Chronic Disease , Humans , Male , Middle Aged , Recurrence , Sweet Syndrome/pathology
2.
Actas Dermosifiliogr ; 97(7): 448-50, 2006 Sep.
Article in Spanish | MEDLINE | ID: mdl-16978543

ABSTRACT

Granuloma annulare is a benign dermatosis of unknown etiology and chronic course, with different clinical variants. The disseminated form predominantly affects the extremities, sparing the trunk. We present the case of a 52-year-old woman with recurrent and autolimited outbreaks of disseminated granuloma annulare that began at summer time and involved the legs, arms and the dorsal area of hands. No pathological findings were observed in the laboratory studies performed. Histopathological examination confirmed our clinical suspicion. The development of granuloma annulare in photoexposed areas and sun exposure as a precipitating factor have been rarely reported in the literature.


Subject(s)
Granuloma Annulare/etiology , Sunlight/adverse effects , Female , Granuloma Annulare/pathology , Humans , Middle Aged
3.
Dermatology ; 194(2): 177-9, 1997.
Article in English | MEDLINE | ID: mdl-9094471

ABSTRACT

We report a case of favus affecting the temporal region of the scalp in a 22-month-old boy. Mycological study of hairs and crusts identified Trichophyton mentagrophytes var. quinckeanum (T. quinckeanum), the causative agent of mouse favus. Treatment with oral griseofulvin led to healing.


Subject(s)
Tinea Favosa/diagnosis , Administration, Oral , Animals , Antifungal Agents/administration & dosage , Antifungal Agents/therapeutic use , Drug Therapy, Combination , Griseofulvin/administration & dosage , Griseofulvin/therapeutic use , Humans , Infant , Male , Mice , Naphthalenes/administration & dosage , Naphthalenes/therapeutic use , Terbinafine , Tinea Favosa/drug therapy , Tinea Favosa/microbiology , Trichophyton/classification
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