Androgen Insensitivity Syndrome with Bilateral Cryptorchidism and Seminoma in Tibet:Report of One Case / 中国医学科学院学报
Acta Academiae Medicinae Sinicae
; (6): 173-176, 2022.
Article
in Zh
| WPRIM
| ID: wpr-927862
Responsible library:
WPRO
ABSTRACT
Androgen insensitivity syndrome(AIS)with bilateral testicular malignant transformation is very rare,and its diagnosis should be based on clinical manifestations,physical examination,serological findings,karyotype analysis,and pathological findings.This study reported a case of complete androgen insensitivity syndrome among Tibetan in Tibet.It took 17 years from the discovery of congenital absence of uterus to bilateral pelvic mass resection.Pathological examination confirmed that bilateral pelvic space occupying lesions were dysplastic testicular tissue with seminoma and sertoli cell adenoma-like nodules.This study summarized the clinicopathological features to deepen the understanding of the disease.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Androgen-Insensitivity Syndrome
/
Testicular Neoplasms
/
Seminoma
/
Tibet
/
Cryptorchidism
Limits:
Female
/
Humans
/
Male
Country/Region as subject:
Asia
Language:
Zh
Journal:
Acta Academiae Medicinae Sinicae
Year:
2022
Type:
Article