Literature DB >> 23845653

Ovarian steroid cell tumor, not otherwise specified, associated with congenital adrenal hyperplasia: rare tumors of an endocrine disease.

Tina T Thomas1, Kimberly R Ruscher, Srinivas Mandavilli, Fabiola Balarezo, Christine M Finck.   

Abstract

Ovarian steroid cell tumors, not otherwise specified (OSCTs), are extremely rare and present a diagnostic challenge when evaluating an ovarian mass. We present a case of such a tumor in a patient with known Congenital Adrenal Hyperplasia (CAH), secondary to 21-hydroxylase deficiency, who was noncompliant with her medications. The workup, diagnosis, and treatment of this rare condition are described.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Congenital adrenal hyperplasia; Endocrine tumors; Ovarian adrenal rest tumors; Ovarian steroid cell tumors; Ovarian tumor

Mesh：

Year:  2013        PMID： 23845653     DOI： 10.1016/j.jpedsurg.2013.04.006

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN： 0022-3468            Impact factor:   2.545


  7 in total

Review 1.  [Ectopia of the adrenal].

Authors:  W Saeger
Journal:  Pathologe       Date:  2018-09       Impact factor: 1.011

2.  Ovarian Adrenal Rest Tumors Undetected by Imaging Studies and Identified at Surgery in Three Females with Congenital Adrenal Hyperplasia Unresponsive to Increased Hormone Therapy Dosage.

Authors:  Hua-Dong Chen; Li-E Huang; Zhi-Hai Zhong; Zhe Su; Hong Jiang; Jing Zeng; Jun-Cheng Liu
Journal:  Endocr Pathol       Date:  2017-06       Impact factor: 3.943

3.  Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria.

Authors:  Asmahane Ladjouze; Malcolm Donaldson; Ingrid Plotton; Nacima Djenane; Kahina Mohammedi; Véronique Tardy-Guidollet; Delphine Mallet; Kamélia Boulesnane; Zair Bouzerar; Yves Morel; Florence Roucher-Boulez
Journal:  Front Endocrinol (Lausanne)       Date:  2022-06-10       Impact factor: 6.055

4.  Successful laparoscopic resection of virilizing ovarian steroid cell tumor, not otherwise specified, in a 22-year-old woman: a case report and evaluation of the steroidogenic pathway.

Authors:  Jun Matsukawa; Toshifumi Takahashi; Yurika Hada; Wataru Kameda; Kuniaki Ota; Mika Fukase; Kyoko Takahashi; Koki Matsuo; Hideki Mizunuma; Satoru Nagase
Journal:  Fukushima J Med Sci       Date:  2019-12-11

5.  Hyperandrogenism, Elevated 17-Hydroxyprogesterone and Its Urinary Metabolites in a Young Woman with Ovarian Steroid Cell Tumor, Not Otherwise Specified: Case Report and Review of the Literature.

Authors:  Felix C K Wong; Angela Z Chan; W S Wong; Angel H W Kwan; Tracy S M Law; Jacqueline P W Chung; Jeffrey S S Kwok; Angel O K Chan
Journal:  Case Rep Endocrinol       Date:  2019-10-27

6.  Morphologic and Molecular Characterization of Adrenals and Adrenal Rest Affected by Congenital Adrenal Hyperplasia.

Authors:  Vipula Kolli; Isabela Werneck da Cunha; SunA Kim; James R Iben; Ashwini Mallappa; Tianwei Li; Alison Gaynor; Steven L Coon; Martha M Quezado; Deborah P Merke
Journal:  Front Endocrinol (Lausanne)       Date:  2021-09-20       Impact factor: 5.555

7.  Ovarian Steroid Cell Tumor Masquerading as Steroid-Unresponsive Congenital Adrenal Hyperplasia.

Authors:  Jane E Driano; Ana L Creo; Seema Kumar; Asma J Chattha; Aida N Lteif
Journal:  AACE Clin Case Rep       Date:  2021-02-17
  7 in total

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