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一名患有先天性17α-羟化酶缺乏症女性的肾上腺髓质脂肪瘤。

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

作者信息

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

出版信息

Arch Pathol Lab Med. 1985 Dec;109(12):1116-7.

PMID:3878142
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.

摘要

据我们所知,本文报告了一例肾上腺髓质脂肪瘤,该病例为第一例与17-羟化酶缺乏相关的病例。这种罕见的良性病变已知与其他内分泌疾病有关。讨论聚焦于促肾上腺皮质激素和/或类固醇持续刺激作为致病因素的可能作用。本病例为支持这一观点增添了证据。

相似文献

1
Adrenal myelolipoma in a woman with congenital 17-hydroxylase deficiency.一名患有先天性17α-羟化酶缺乏症女性的肾上腺髓质脂肪瘤。
Arch Pathol Lab Med. 1985 Dec;109(12):1116-7.
2
[A case of adrenal myelolipoma associated with adrenogenital syndrome].
Hinyokika Kiyo. 1990 Jan;36(1):35-9.
3
[Problems posed by the association of hemophilia A and congenital adrenal hyperplasia caused by 21-hydroxylase deficiency].
Pediatrie. 1986 Oct-Nov;41(7):559-64.
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Adrenal myelolipoma associated with congenital adrenal 21-hydroxylase deficiency.
Intern Med. 1992 Jun;31(6):803-6. doi: 10.2169/internalmedicine.31.803.
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[Deficiency of 17 alpha-hydroxylase. Presentation of 3 new cases].
Med Clin (Barc). 1984 Mar 10;82(9):407-9.
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Evidence of 11 beta-hydroxylase deficiency in a patient with cortical adrenal adenoma.皮质肾上腺腺瘤患者存在11β-羟化酶缺乏的证据。
Horm Metab Res. 1989 May;21(5):272-4. doi: 10.1055/s-2007-1009210.
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[Hirsutism secondary to congenital adrenal hyperplasia caused by a 21-hydroxylase deficiency of late onset. A clinical case].
Rev Chil Obstet Ginecol. 1984;49(5):295-9.
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[Virilization caused by 21-hydroxylase deficiency and axillary sweat gland hyperplasia].
Ann Dermatol Venereol. 1988;115(11):1136-8.
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Late-occurring giant adrenal myelolipoma in a patient with congenital adrenal hyperplasia.先天性肾上腺增生症患者晚期出现的巨大肾上腺髓质脂肪瘤。
Endocrinol Nutr. 2013 Nov;60(9):e33-4. doi: 10.1016/j.endonu.2012.09.017. Epub 2013 Aug 18.
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Myelolipoma and endocrine dysfunction.
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引用本文的文献

1
Seventeen Alpha-Hydroxylase Deficiency Associated with Absent Gonads and Myelolipoma: A Case Report and Review of Literature.17α-羟化酶缺乏症伴性腺缺如及肾上腺髓质脂肪瘤:一例报告并文献复习
Iran J Med Sci. 2016 Nov;41(6):543-547.
2
Lack of ACTH and androgen receptor expression in a giant adrenal myelolipoma associated with 21-hydroxylase deficiency.与21-羟化酶缺乏相关的巨大肾上腺髓质脂肪瘤中促肾上腺皮质激素(ACTH)和雄激素受体表达缺失。
Endocr Pathol. 2008 Summer;19(2):122-7. doi: 10.1007/s12022-008-9034-2.
3
Lipomatous Changes in Adrenocortical Adenomas: Report of Two Cases.
Endocr Pathol. 1996 Autumn;7(3):223-228. doi: 10.1007/BF02739925.
4
Adrenal myelolipoma: a case report and review of the literature.肾上腺髓脂肪瘤:一例报告并文献复习
Jpn J Surg. 1989 Sep;19(5):597-606. doi: 10.1007/BF02471670.