Coexistence of Ovarian Granulose Cell Tumor, Congenital Adrenal

Purpose Congenital adrenal hyperplasia (CAH) is rare autosomal recessive disease. CAH due to 21-hydroxylase deficiency accounts for 95% of cases. We aimed to share the first case of coexistence of simple virilizing-type congenital adrenal hyperplasia [I172N mutation in the CYP21A], triple translocat...

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Main Authors: Akbulut, S, Ceylan, SD, Tuncali, T, Sogutcu, N
Language:unknown
Published: 2021
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Online Access:http://hdl.handle.net/11616/23739
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spelling ftinonuuniv:oai:abakus.inonu.edu.tr:11616/23739 2023-05-15T18:11:58+02:00 Coexistence of Ovarian Granulose Cell Tumor, Congenital Adrenal Hyperplasia, and Triple Translocation: Is a Consequence or Coincidence? Akbulut, S Ceylan, SD Tuncali, T Sogutcu, N 2021-03-31T11:12:48Z http://hdl.handle.net/11616/23739 unknown http://hdl.handle.net/11616/23739 JOURNAL OF GASTROINTESTINAL CANCER 2021 ftinonuuniv 2022-03-28T19:51:35Z Purpose Congenital adrenal hyperplasia (CAH) is rare autosomal recessive disease. CAH due to 21-hydroxylase deficiency accounts for 95% of cases. We aimed to share the first case of coexistence of simple virilizing-type congenital adrenal hyperplasia [I172N mutation in the CYP21A], triple translocation [t(9;11;12)], and ovarian granulose cell tumor. Methods A 59-year-old female patient was presented to our clinic, complaining with abdominal pain and distension. Physical examination revealed palpable abdominal mass, virilism, ambiguous genitalia, clitoramegaly, and hyperpigmentation. Contrast-enhanced abdominal computed tomography showed a giant mass originating from the right tubo-ovarian structure. Results The patient was operated in the light of the clinico-radiological features mentioned above. A giant mass weighing 3500 g was detected on the right tubo-ovarian structure during laparotomy, and mass was excised with right tubo-ovarian structure. Immunohistochemical examination revealed ovarian granulosa cell tumor. The high serum concentration of 17-OH progesterone was measured at baseline and after 250-mu g bolus of synthetic ACTH. In genetic analysis, we screened for six-point mutations, large deletions, and non-common mutations using restriction fragment length polymorphism (RFLP) methods, PCR, and sequencing of CYP21 gene respectively. The patient was detected to be homozygous for the I172N mutation. In addition, 50% of the metaphases examined had triple translocation [t(9;11;12)]. Conclusion The coexistence of congenital adrenal hyperplasia, triple chromosomal translocations, and ovarian granulosa cell tumor has not been described previously. This coexistence may be a sign of a new syndrome. C1 [Akbulut, Sami] Inonu Univ, Fac Med, Dept Surg, Elazig Yolu 10 Km, TR-44280 Malatya, Turkey. [Akbulut, Sami] Inonu Univ, Fac Med, Liver Transplant Inst, Elazig Yolu 10 Km, TR-44280 Malatya, Turkey. [Ceylan, Senay Durmaz] Kirikkale Univ, Dept Endocrinol, Fac Med, TR-71450 Kirikkale, Turkey. [Tuncali, Timur] Ankara Univ, Dept Genet, Fac Med, TR-06100 Ankara, Turkey. [Sogutcu, Nilgun] Diyarbakir Educ & Res Hosp, Dept Pathol, TR-21400 Diyarbakir, Turkey. Other/Unknown Material sami Unknown
institution Open Polar
collection Unknown
op_collection_id ftinonuuniv
language unknown
description Purpose Congenital adrenal hyperplasia (CAH) is rare autosomal recessive disease. CAH due to 21-hydroxylase deficiency accounts for 95% of cases. We aimed to share the first case of coexistence of simple virilizing-type congenital adrenal hyperplasia [I172N mutation in the CYP21A], triple translocation [t(9;11;12)], and ovarian granulose cell tumor. Methods A 59-year-old female patient was presented to our clinic, complaining with abdominal pain and distension. Physical examination revealed palpable abdominal mass, virilism, ambiguous genitalia, clitoramegaly, and hyperpigmentation. Contrast-enhanced abdominal computed tomography showed a giant mass originating from the right tubo-ovarian structure. Results The patient was operated in the light of the clinico-radiological features mentioned above. A giant mass weighing 3500 g was detected on the right tubo-ovarian structure during laparotomy, and mass was excised with right tubo-ovarian structure. Immunohistochemical examination revealed ovarian granulosa cell tumor. The high serum concentration of 17-OH progesterone was measured at baseline and after 250-mu g bolus of synthetic ACTH. In genetic analysis, we screened for six-point mutations, large deletions, and non-common mutations using restriction fragment length polymorphism (RFLP) methods, PCR, and sequencing of CYP21 gene respectively. The patient was detected to be homozygous for the I172N mutation. In addition, 50% of the metaphases examined had triple translocation [t(9;11;12)]. Conclusion The coexistence of congenital adrenal hyperplasia, triple chromosomal translocations, and ovarian granulosa cell tumor has not been described previously. This coexistence may be a sign of a new syndrome. C1 [Akbulut, Sami] Inonu Univ, Fac Med, Dept Surg, Elazig Yolu 10 Km, TR-44280 Malatya, Turkey. [Akbulut, Sami] Inonu Univ, Fac Med, Liver Transplant Inst, Elazig Yolu 10 Km, TR-44280 Malatya, Turkey. [Ceylan, Senay Durmaz] Kirikkale Univ, Dept Endocrinol, Fac Med, TR-71450 Kirikkale, Turkey. [Tuncali, Timur] Ankara Univ, Dept Genet, Fac Med, TR-06100 Ankara, Turkey. [Sogutcu, Nilgun] Diyarbakir Educ & Res Hosp, Dept Pathol, TR-21400 Diyarbakir, Turkey.
author Akbulut, S
Ceylan, SD
Tuncali, T
Sogutcu, N
spellingShingle Akbulut, S
Ceylan, SD
Tuncali, T
Sogutcu, N
Coexistence of Ovarian Granulose Cell Tumor, Congenital Adrenal
author_facet Akbulut, S
Ceylan, SD
Tuncali, T
Sogutcu, N
author_sort Akbulut, S
title Coexistence of Ovarian Granulose Cell Tumor, Congenital Adrenal
title_short Coexistence of Ovarian Granulose Cell Tumor, Congenital Adrenal
title_full Coexistence of Ovarian Granulose Cell Tumor, Congenital Adrenal
title_fullStr Coexistence of Ovarian Granulose Cell Tumor, Congenital Adrenal
title_full_unstemmed Coexistence of Ovarian Granulose Cell Tumor, Congenital Adrenal
title_sort coexistence of ovarian granulose cell tumor, congenital adrenal
publishDate 2021
url http://hdl.handle.net/11616/23739
genre sami
genre_facet sami
op_source JOURNAL OF GASTROINTESTINAL CANCER
op_relation http://hdl.handle.net/11616/23739
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