A 68-Year-Old Phenotypically Male Patient with 21-Hydroxylase Deficiency and Concomitant Adrenocortical Neoplasm Producing Testosterone and Cortisol

被引:8
作者
Hayashi, Masayuki [1 ]
Kataoka, Yuko [1 ]
Sugimura, Yoshihisa [2 ]
Kato, Fumiko [3 ,4 ]
Fukami, Maki [3 ]
Ogata, Tsutomu [3 ,4 ]
Homma, Keiko [5 ]
Hasegawa, Tomonobu [6 ]
Oiso, Yutaka [2 ]
Sasano, Hironobu [7 ]
Tanaka, Hiroshi [1 ]
机构
[1] Chukyo Hosp, Dept Endocrinol & Metab, Nagoya, Aichi 4578510, Japan
[2] Nagoya Univ, Grad Sch Med, Field Internal Med, Dept Endocrinol & Diabet, Nagoya, Aichi 4648601, Japan
[3] Natl Res Inst Child Hlth & Dev, Dept Mol Endocrinol, Tokyo, Japan
[4] Hamamatsu Univ Sch Med, Dept Pediat, Hamamatsu, Shizuoka 4313192, Japan
[5] Keio Univ Hosp, Cent Clin Labs, Tokyo, Japan
[6] Keio Univ, Sch Med, Dept Pediat, Tokyo, Japan
[7] Tohoku Univ, Grad Sch Med, Dept Pathol, Sendai, Miyagi 980, Japan
关键词
adrenocortical carcinoma; cortisol; 21-hydroxylase deficiency; prominent masculinization; testosterone; STEROID; 21-HYDROXYLASE; JAPANESE PATIENTS; GENE; MUTATIONS; EXPRESSION; DIAGNOSIS; HYPERPLASIA; COMPLEMENT; COMPONENT; INFANTS;
D O I
10.1620/tjem.231.75
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The steroidogenic enzyme 21-hydroxylase is necessary for the synthesis of both glucocorticoids and mineralocorticoids. 21-hydroxylase is a cytochrome P-450 enzyme and is encoded by the gene CYP21A2. Here we report a 68-year-old phenotypically 'male' but genetically female patient with 21-hydroxylase deficiency (21OHD) and the concomitant virilizing adrenocortical carcinoma. This patient grew up as a male and has not encountered any episodes of adrenal insufficiency without glucocorticoid replacement in his lifetime. A chromosome test at admission, however, identified the 46, XX karyotype, and serum 17-hydroxyprogesterone and urine pregnanetriolone and 11 beta-hydroxyandrostendione were all elevated, consistent with 210HD. Moreover, serum testosterone was 1.90 ng/ml, much higher than the female standard levels, and serum cortisol was 5.7 mu g/ml, slightly lower than standard levels. Genetic analysis identified the patient as a heterozygote of the two pathogenic mutations in the CYP21A2 gene: IVS2-13C(A)>G and R356W. Magnetic resonance imaging (MRI) revealed the presence of left adrenal tumor measuring 6 cm, which was subsequently diagnosed as adrenocortical carcinoma based on the criteria of Weiss. Immunohistochemical analysis of the tumor specimens revealed the expression of various enzymes involved in testosterone production, including 3 beta-hydroxysteroid dehydrogenase, 17 alpha-hydroxylase/17,20-lyase, and 17 beta-hydroxysteroid dehydrogenase. Importantly, the expression of immunoreactive 21-hydroxylase was detected in these tumor cells. The levels of adrenal tumor-derived steroid metabolites were all markedly decreased following the surgery. This is the first report on a virilized 21OHD patient associated with the adrenocortical tumor that produces testosterone. Moreover, the concomitant adrenocortical tumor may ameliorate adrenocortical insufficiency by producing cortisol.
引用
收藏
页码:75 / 84
页数:10
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