Literature DB >> 24834391

Testicular adrenal rest tumor mimicking leydig cell tumor in a patient with congenital adrenal hyperplasia.

Esra Karakuş1, Müjdem Nur Azılı2, Tuğrul Tiryaki2.   

Abstract

Entities:  

Year:  2014        PMID: 24834391      PMCID: PMC4005084     

Source DB:  PubMed          Journal:  APSP J Case Rep        ISSN: 2218-8185


× No keyword cloud information.
Dear Sir, A 7-year-old boy, known case of CAH, was referred to our hospital with bilateral testicular enlargement. On examination, hyperpigmentation of the scrotum was observed. In addition, ultrasound (US) of testicles revealed round-to-oval hypoechoic heterogeneous lesions [34x14 mm (right) and 19x7 mm (left)]. The patient underwent testicular sparing tumor enucleation. On macroscopic examination the nodules were well-circumscribed, encapsulated, firm, and yellow in color (Fig. 1). Microscopic evaluation revealed that the tumors were composed of polygonal cells with abundant eosinophilic cytoplasm and well-defined borders (Fig. 2). The tumor cells were separated by a fibrous stroma. There were no evidences of infiltrating margins, necrosis, nuclear atypia, or vascular invasion. There was also no evidence of Reinke’s crystals. Figure 1: On gross examination the nodules appeared encapsulated, firm, and yellow in color Figure 2: Tumor composed of polygonal cells with abundant eosinophilic cytoplasm and well-defined borders (X 400 H/E) Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder characterized by enzyme defects in the steroidogenic pathways. Testicular adrenal rest tumors (TARTs) are may have serious consequences in patients with CAH. They probably develop from ectopic remnants of intratesticular adrenal tissue, which might be stimulated by the rise of adrenocorticotropic hormone (ACTH). Their histological differentiation from Leydig-cell tumors is extremely difficult.[1] Testicular masses may be encountered in CAH patients which may lead to gonadal failure. These are bilateral lesions and are also called TART which do regresss after steroid therapy. Histopathologically they may be confused with Leydig cell tumors. TARTs are observed in young adults but are negative for Reinke crystals which are observed in Leydig cell tumors. Definitive diagnosis can be made by clinical, laboratory and endocrinological evaluations.[2,3]

Footnotes

Source of Support: Nil Conflict of Interest: None declared
  3 in total

Review 1.  Testicular adrenal rest tumours in boys with congenital adrenal hyperplasia: case report and literature review.

Authors:  Elżbieta Budzyńska; Iwona Beń-Skowronek
Journal:  Pediatr Endocrinol Diabetes Metab       Date:  2011

2.  Leydig cell tumor in two brothers with congenital adrenal hyperplasia due to 11-β hydroxylase deficiency: a case report.

Authors:  Pegah Entezari; Abdol Mohammad Kajbafzadeh; Fatemeh Mahjoub; Mohammad Vasei
Journal:  Int Urol Nephrol       Date:  2011-01-23       Impact factor: 2.370

3.  Testicular adrenal rest tumors in patients with congenital adrenal hyperplasia.

Authors:  Esra Deniz Papatya Çakir; Fatma Sentürk Mutlu; Erdal Eren; Aliye Ozlem Paşa; Halil Sağlam; Omer Tarim
Journal:  J Clin Res Pediatr Endocrinol       Date:  2012-06
  3 in total
  1 in total

1.  An Association of Chronic Hyperaldosteronism with Medullary Nephrocalcinosis.

Authors:  Kartik Mittal; Karan Anandpara; Amit K Dey; Rajaram Sharma; Hemangini Thakkar; Priya Hira; Hemant Deshmukh
Journal:  Pol J Radiol       Date:  2015-09-05
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.