Organ-sparing surgery of the bilateral testicular large cell calcifying sertoli cell tumor in patient with atypical Peutz–Jeghers syndrome

التفاصيل البيبلوغرافية
العنوان: Organ-sparing surgery of the bilateral testicular large cell calcifying sertoli cell tumor in patient with atypical Peutz–Jeghers syndrome
المؤلفون: W. Cichy, A. Plawski, B. S. Lipska, A. Gintowt, A. Kaluzny, Marcin Matuszewski, K. Krajka, S. Wojtylak
المصدر: International Urology and Nephrology
بيانات النشر: Springer Science and Business Media LLC, 2011.
سنة النشر: 2011
مصطلحات موضوعية: Male, Pathology, medicine.medical_specialty, Urology, Peutz-Jeghers Syndrome, STK11, Peutz–Jeghers syndrome, Protein Serine-Threonine Kinases, Testicle, Large cell calcifying sertoli cell tumor, Diagnosis, Differential, Young Adult, AMP-Activated Protein Kinase Kinases, Testicular Neoplasms, Calcinosis, medicine, Organ-sparing testicular surgery, Humans, Carney complex, business.industry, Nucleic acid amplification technique, medicine.disease, medicine.anatomical_structure, Nephrology, Sertoli Cell Tumor, Urology – Case Report, Differential diagnosis, STK11 amplification, business, Nucleic Acid Amplification Techniques, Orchiectomy
الوصف: Large cell calcifying sertoli cell tumor (LCCSCT) is an exceptionally rare neoplasm originating from sperm cord cells. The tumors have relatively low malignant potential and unlikely proceed to metastasis formation. The lesions may occur in an isolated form or in ca. 40% of cases may be associated with genetic abnormalities, by and large Peutz-Jeghers syndrome and Carney complex. At presentation, 20% of LCCSCT cases are bilateral and/or multifocal. Owning to characteristic skin lesions and particular hyperechoic ultrasound image of the tumor, preliminary diagnosis of the syndromic LCCSCT is possible in the preoperative period. Consequently, testicle organ-sparing procedure can be attempted, which is especially justified in bilateral lesions. Here, we report a case of a bilateral LCCSCT in a 20-year-old man with atypical Peutz-Jeghers syndrome due to amplification of the exon 1 of STK11 gene who was successfully treated with bilateral testicle-sparing tumorectomies.
تدمد: 1573-2584
0301-1623
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55b7eb6f55eb43291e8527b3475da317
https://doi.org/10.1007/s11255-011-0100-1
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....55b7eb6f55eb43291e8527b3475da317
قاعدة البيانات: OpenAIRE