Literature DB >> 3878142

Adrenal myelolipoma in a woman with congenital 17-hydroxylase deficiency.

E Condom, C M Villabona, J M Gómez, M Carrera.   

Abstract

A case of adrenal myelolipoma, which to our knowledge is the first case to be associated with 17-hydroxylase deficiency, is reported. This rare, benign lesion is known to occur in association with other endocrinopathies. Discussion focuses on the possible role of continued stimulation by corticotropin and/or steroids as pathogenic factors. The present case adds evidence supporting this view.

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Year:  1985        PMID: 3878142

Source DB:  PubMed          Journal:  Arch Pathol Lab Med        ISSN: 0003-9985            Impact factor:   5.534


  4 in total

1.  Lack of ACTH and androgen receptor expression in a giant adrenal myelolipoma associated with 21-hydroxylase deficiency.

Authors:  Hanae Hagiwara; Takeshi Usui; Takashi Kimura; Tetsuya Tagami; Mitsuhide Naruse; Sachiko Minamiguchi; Takuma Kato; Hiroshi Okuno; Akira Shimatsu
Journal:  Endocr Pathol       Date:  2008       Impact factor: 3.943

2.  Lipomatous Changes in Adrenocortical Adenomas: Report of Two Cases.

Authors:  Mauro Papotti; Anna Sapino; Enrico Mazza; Sergio Sandrucci; Marco Volante; Gianni Bussolati
Journal:  Endocr Pathol       Date:  1996       Impact factor: 3.943

Review 3.  Adrenal myelolipoma: a case report and review of the literature.

Authors:  T Tanaka; N Matsuo; H Ishikura; D Takagi; N Takeyama
Journal:  Jpn J Surg       Date:  1989-09

4.  Seventeen Alpha-Hydroxylase Deficiency Associated with Absent Gonads and Myelolipoma: A Case Report and Review of Literature.

Authors:  Mahmood Soveid; Ghanbar Ali Rais-Jalali
Journal:  Iran J Med Sci       Date:  2016-11
  4 in total

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