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1.
Emerg Infect Dis ; 26(10): 2518-2520, 2020 10.
Artículo en Inglés | MEDLINE | ID: mdl-32946726

RESUMEN

We investigated palatine tonsil and adenoid specimens excised from otorhinolaryngological patients in a leprosy-endemic region of Brazil. Fite-Faraco staining identified Mycobacterium spp. in 9 of 397 specimen blocks. Immunohistochemistry and molecular analysis confirmed the presence of Mycobacterium leprae, indicating that these organs can house M. leprae in persons inhabiting a leprosy-endemic region.


Asunto(s)
Tonsila Faríngea , Lepra , Brasil/epidemiología , Humanos , Lepra/epidemiología , Mycobacterium leprae/genética , Tonsila Palatina
2.
J Infect Dev Ctries ; 6(6): 526-30, 2012 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-22711134

RESUMEN

Epidermodysplasia verruciformis (EV) is triggered by a variety of mechanisms that at least partly include genetic background. We present a Brazilian man with a 30-year history of flat, wart-like lesions with clinical, histopathological, and evolutive aspects consistent with papillomavirus (HPV)-associated EV. Histological analysis of the wart lesions showed epidermis with hyperkeratosis, regular acanthosis, hypergranulosis, and cells with abundant basophilic cytoplasm. Moreover, a perivascular lymphocytic infiltrate was found in the superficial dermis, consistent with a viral wart. Type-2-HPV DNA was detected in various fragments of skin-wart lesions using the polymerase chain reaction (PCR). Two years after the EV diagnosis, the patient presented with an anesthetic well-demarcated, erythematous and mildly scaly plaque on his right forearm. A histopathological analysis of this lesion demonstrated the presence of a compact tuberculoid granuloma. Ziehl-Neelsen staining demonstrated the presence of rare acid-fast bacilli and confirmed the tuberculoid leprosy diagnosis. The patient's Mitsuda Intradermal Reaction was positive. To elucidate the possible mechanism involved in this case of EV, we genotyped the HLA genes of this patient. DQB genotyping showed the polymorphic HLA alleles DQB1*0301 and 0501. The patient was treated with a paucibacillary multi-drug therapy scheme, and the disease was cured in six months. This report describes an EV patient with an M. leprae infection, confirming that tuberculoid leprosy patients possess a relatively specific and efficient cell-mediated immunity against the bacillus and, therefore, localized forms of the disease. Moreover, we show the possible involvement of the polymorphic HLA alleles DQB1*0301 and 0501 in EV induction mechanisms.


Asunto(s)
Epidermodisplasia Verruciforme/complicaciones , Epidermodisplasia Verruciforme/patología , Lepra Tuberculoide/diagnóstico , Lepra Tuberculoide/patología , Antibacterianos/administración & dosificación , Brasil , ADN Viral/genética , ADN Viral/aislamiento & purificación , Epidermodisplasia Verruciforme/virología , Cadenas beta de HLA-DQ/genética , Histocitoquímica , Humanos , Lepra Tuberculoide/tratamiento farmacológico , Masculino , Microscopía , Persona de Mediana Edad , Papillomaviridae/clasificación , Papillomaviridae/aislamiento & purificación , Infecciones por Papillomavirus/complicaciones , Infecciones por Papillomavirus/patología , Reacción en Cadena de la Polimerasa , Piel/patología , Pruebas Cutáneas , Resultado del Tratamiento
3.
Pediatr Dermatol ; 20(3): 215-20, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12787269

RESUMEN

Granular parakeratosis is a cutaneous eruption with erythematous and/or brownish hyperkeratotic papules and plaques which are exclusively localized to intertriginous areas and show histopathologic features of an unusual form of parakeratosis. The etiology is unknown, but the excessive use of various topical preparations (e.g., ointments and deodorants) has been associated with this disease. It has heretofore been reported only in adults. We report two children, ages 3 and 5 months, with characteristic lesions in the groin associated with topical pomades used to prevent diaper rash. This is the first report associating the clinical presentation and the histopathologic diagnosis of granular parakeratosis in children. The literature on this entity is also reviewed and all case reports are summarized.


Asunto(s)
Paraqueratosis/patología , Biopsia con Aguja , Femenino , Humanos , Inmunohistoquímica , Lactante , Remisión Espontánea , Índice de Severidad de la Enfermedad
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