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[Intravenous leiomyomatosis]. / Die intravenöse Leiomyomatose.
Kommoss, F; Ebel, T; Drusenheimer, J; Schelzig, H; Lichtenberg, A; Fehm, T; Aubin, H.
Afiliação
  • Kommoss F; Pathologisches Institut, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 224, 69120, Heidelberg, Deutschland. felix.kommoss@med.uni-heidelberg.de.
  • Ebel T; Zentrum für Pathologie Essen-Mitte, Essen, Deutschland.
  • Drusenheimer J; Institut für Pathologie, Universitätsklinikum Düsseldorf, Düsseldorf, Deutschland.
  • Schelzig H; Klinik für Gefäß- und Endovaskularchirurgie, Universitätsklinikum Düsseldorf, Düsseldorf, Deutschland.
  • Lichtenberg A; Klinik für Kardiovaskuläre Chirurgie, Universitätsklinikum Düsseldorf, Düsseldorf, Deutschland.
  • Fehm T; Klinik für Frauenheilkunde und Geburtshilfe, Universitätsklinikum Düsseldorf, Düsseldorf, Deutschland.
  • Aubin H; Klinik für Kardiovaskuläre Chirurgie, Universitätsklinikum Düsseldorf, Düsseldorf, Deutschland.
Pathologe ; 40(1): 80-84, 2019 Feb.
Article em De | MEDLINE | ID: mdl-30680436
Intravenous leiomyomatosis (IVLM) is an unusual neoplasm derived from uterine smooth muscle cells seen in patients with uterine leiomyomas. The typical histological features of IVLM consist of benign smooth muscle cells present within venous vascular spaces of the uterine wall. Increasing intravascular and intracardial spread of IVLM may lead to life-threatening clinical complications. Thorough pathological study of routine hysterectomy specimens may lead to the diagnosis of IVLM. Most affected patients will be cardiologically asymptomatic at the time of diagnosis. Herein, the relatively unknown clinical and morphological aspects of IVLM are presented and discussed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Uterinas / Leiomiomatose Limite: Female / Humans Idioma: De Revista: Pathologe Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Uterinas / Leiomiomatose Limite: Female / Humans Idioma: De Revista: Pathologe Ano de publicação: 2019 Tipo de documento: Article
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