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pubmed-article:17204109pubmed:abstractTextOur patient was a 77-year-old Japanese woman, who was under treatment for idiopathic thrombocytopenic purpura (ITP) and chronic renal failure. She had warm nodules and cord-like induration on her left knee that appeared similar to Bazin's erythema induratum. A chest X-ray examination revealed miliary tuberculosis; after anti-mycobacterial therapy, the warm nodules and cord-like induration were transformed into a cold, non-tender abscess that drained. Histopathological findings showed caseation necrosis in the subcutaneous tissue, however, mycobacteria were directly detected by Ziehl-Neelsen staining from cutaneous lesions, and cultures from the same lesion also grew Mycobacterium tuberculosis. Tuberculous gumma demonstrated multiple, cold, painless abscesses and thrombosis were also seen. This is a rare and unusual clinical form of cutaneous tuberculosis, and the result of hematogenous dissemination from a primary focus during periods of lowered resistance.lld:pubmed
pubmed-article:17204109pubmed:languageenglld:pubmed
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pubmed-article:17204109pubmed:authorpubmed-author:TakedaHiroshi...lld:pubmed
pubmed-article:17204109pubmed:authorpubmed-author:KatsuokaKense...lld:pubmed
pubmed-article:17204109pubmed:authorpubmed-author:AraiSatoruSlld:pubmed
pubmed-article:17204109pubmed:authorpubmed-author:MaejimaHideki...lld:pubmed
pubmed-article:17204109pubmed:authorpubmed-author:EbataToshiyaTlld:pubmed
pubmed-article:17204109pubmed:authorpubmed-author:KusunokiMaiMlld:pubmed
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pubmed-article:17204109pubmed:volume34lld:pubmed
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pubmed-article:17204109pubmed:year2007lld:pubmed
pubmed-article:17204109pubmed:articleTitleTuberculous gumma associated with idiopathic thrombocytopenic purpura: report of a Japanese female patient.lld:pubmed
pubmed-article:17204109pubmed:affiliationDepartment of Dermatology, Kitasato University School of Medicine, Sagamihara, Kanagawa, and Daisan Hospital, Tokyo, Japan. hm4765@yahoo.co.jplld:pubmed
pubmed-article:17204109pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:17204109pubmed:publicationTypeCase Reportslld:pubmed