The Many Faces of Cardiac Sarcoidosis.

Objectives: The objective of this study was to review and illustrate the sometimes diagnostically challenging features of cardiac sarcoidosis. We emphasize variable phenotypes presented at explant and biopsy evaluation and review literature regarding ancillary clinical and pathologic studies to enha...

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Publicado en:American Journal of Clinical Pathology Vol. 153; no. 3; pp. 294 - 303
Autores principales: Serei, Virian D, Fyfe, Billie
Formato: pictorial review Journal Article
Publicado: Oxford University Press / USA Mar2020
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Mar2020
      vid: 153
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      pub: Oxford University Press / USA
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        atl: The Many Faces of Cardiac Sarcoidosis.
      aug:
        au:
          Serei, Virian D
          Fyfe, Billie
        affil: Department of Pathology and Laboratory Medicine, Rutgers-Robert Wood Johnson Medical School, New Brunswick, NJ
      sug:
        subj:
          Myocardial Diseases Diagnosis
          Sarcoidosis Diagnosis
          Myocardium Pathology
          Macrophages Pathology
          Sarcoidosis Pathology
          Human
          Granuloma Pathology
          Myocardial Diseases Pathology
      ab: Objectives: The objective of this study was to review and illustrate the sometimes diagnostically challenging features of cardiac sarcoidosis. We emphasize variable phenotypes presented at explant and biopsy evaluation and review literature regarding ancillary clinical and pathologic studies to enhance diagnostic accuracy.Methods: A literature review was performed and two cardiac sarcoidosis cases were illustrated.Results: Our cases and literature review demonstrate the pathologic spectrum of cardiac sarcoidosis. Irregular left ventricular free wall involvement is most common, followed by the interventricular septum and right ventricle. Although granulomas are often composed of tight epithelioid macrophage aggregates, early granulomas comprise loosely associated macrophages with lymphocyte predominance. Chronic disease leads to fibrosis and end-stage heart failure. Sampling errors and variable histology cause low endomyocardial biopsy sensitivity.Conclusions: Current guidelines use clinical, radiologic, and immunohistologic criteria for diagnosing cardiac sarcoidosis. Knowledge of these guidelines will assist pathologists in making accurate diagnosis of this disease.
      pubtype: Academic Journal
      doctype:
        pictorial
        review
        Journal Article
      ougenre: Article
    language: English
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