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1.
Dermatol Online J ; 23(10)2017 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-29469779

RESUMO

(no more than 200 words): In the last few years, the incidence of cutaneous infections caused by nontuberculous mycobacteria is increasing. Since Mycobacterium immunogenum was first described in 2001, few case reports have been described, all of them in the American continent. We report a case with cutaneous infection caused by this newly discovered NTB in Europe.A 65-year-old woman presented with a 3-months history of pruritic lesions on abdomen. Examination revealed erythematous inflammatory papules, pustules, and crusts. Three weeks later, mycobacteria were cultured from the biopsy specimen. Mycobacterium immunogenum was identified based on susceptibility test results and polymerase chain reaction (PCR) restriction enzyme analysis. Treatment with clarithromycin was started. M. immunogenum is a nontuberculous mycobacterium that was first described by Wilson et al. in 2001 as a rapidly growing variety and new species in the Mycobacterium chelonae-Mycobacterium abscessus group. PCR-restriction analysis of a 439-bp segment of the hsp65 gene and/or sequencing the species-specific region of the 16S rDNA can confirm this new species. Since the description of M. immunogenum, 8 clinical case reports have been published, most involving cutaneous infections and all of them in the American continent. We present a case of cutaneous infection caused by M. immunogenum in a Spanish woman.


Assuntos
Infecções por Mycobacterium/microbiologia , Micobactérias não Tuberculosas/isolamento & purificação , Dermatopatias Bacterianas/microbiologia , Idoso , Antibacterianos/uso terapêutico , Claritromicina/uso terapêutico , DNA Bacteriano/isolamento & purificação , Feminino , Humanos , Infecções por Mycobacterium/tratamento farmacológico , Infecções por Mycobacterium/patologia , Micobactérias não Tuberculosas/genética , Reação em Cadeia da Polimerase , Dermatopatias Bacterianas/tratamento farmacológico , Dermatopatias Bacterianas/patologia , Espanha
2.
Dermatol Online J ; 17(11): 4, 2011 Nov 15.
Artigo em Inglês | MEDLINE | ID: mdl-22136860

RESUMO

In 1988, Tumiati et al described the first case of calcinosis cutis related to a calcium-containing heparin. Since then, only 18 cases have been reported in the literature; they usually have an altered calcium-phosphate product, an elevated parathyroid hormone (PTH), or both. We report a 33-year-old patient who developed calcinosis cutis at sites of nadroparin injections without any disturbance of calcium-phosphate product, PTH, or vitamin D. The pathogenesis of calcinosis cutis secondary to nadroparin injections remains controversial; Proposed causes included metastatic, dystrophic, iatrogenic, or multifactorial etiologies. This is the first case of multiple nodules of calcinosis cutis without alterations of calcium-phosphate product, PTH, or vitamin D, which supports an iatrogenic mechanism. We also suggest that calcinosis cutis could be more frequent than we thought and is probably an underdiagnosed entity.


Assuntos
Anticoagulantes/efeitos adversos , Calcinose/induzido quimicamente , Nadroparina/efeitos adversos , Dermatopatias/induzido quimicamente , Adulto , Amiodarona/uso terapêutico , Anticoagulantes/administração & dosagem , Fibrilação Atrial/tratamento farmacológico , Biópsia , Calcinose/patologia , Cálcio/análise , Enoxaparina/uso terapêutico , Humanos , Injeções Subcutâneas , Masculino , Nadroparina/administração & dosagem , Dermatopatias/patologia
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