Normal pelvic ultrasound or MRI does not rule out neoplasm in patients with gonadal dysgenesis and Y chromosome material

2018 ◽  
Vol 14 (2) ◽  
pp. 154.e1-154.e6 ◽  
Author(s):  
Kristin M. Ebert ◽  
Geri D. Hewitt ◽  
Justin A. Indyk ◽  
Katherine A. McCracken ◽  
Leena Nahata ◽  
...  
Author(s):  
Lindsey Guzewicz ◽  
Susan Howell ◽  
Canice E. Crerand ◽  
Hailey Umbaugh ◽  
Natalie J. Nokoff ◽  
...  

1991 ◽  
Vol 1 (3) ◽  
pp. 141-143 ◽  
Author(s):  
M. A. Steller ◽  
J. T. Soper ◽  
C. A. Szpak ◽  
J. T. Lanman ◽  
D. L. Clark-Pearson

Gonadal dysgerminomas developed in two girls, aged 12 and 15 years. Both were initially treated with conservative unilateral gonadectomy. Forty-six, XY gonadal dysgenesis was not suspected in either patient due to the normal appearance of the contralateral gonads and internal female genital organs. One died of a second germ cell malignancy which developed in the contralateral ovary 9½ years later. The diagnosis of 46, XY gonadal dysgenesis was established by karyotype in both patients. Although conservative surgical management is desirable for nulliparous women with unilateral dysgerminomas, the presence of 46, XY gonadal dysgenesis should be suspected in all premenarchal girls with ovarian germ cell malignancies. If karyotyping reveals the presence of an Y chromosome, bilateral gonadectomy is indicated because of the risk that another neoplasm may develop in the contralateral ovary.


1980 ◽  
Vol 136 (5) ◽  
pp. 639-645 ◽  
Author(s):  
W.R.Scott Curtis ◽  
Beverly J. White ◽  
Anne W. Lucky ◽  
Nan Roche-Bender ◽  
Douglas R. Knab ◽  
...  

2000 ◽  
Vol 85 (9) ◽  
pp. 3199-3202 ◽  
Author(s):  
Claus Højbjerg Gravholt ◽  
Jens Fedder ◽  
Rune Weis Naeraa ◽  
Jørn Müller

Abstract The presence of Y chromosome material in patients with Turner syndrome is a risk factor for the development of gonadoblastoma. However, no cases with gonadoblastoma or other ovarian malignancies have been found in epidemiological studies of cancer, morbidity, or mortality in Turner syndrome. We examined 114 females with Turner syndrome for the presence of Y chromosome material by PCR. Initially, five different primer sets were used. Y Chromosome-positive individuals were further examined with an additional four primer sets. We found 14 (12.2%; 95% confidence interval, 6.9–19.7%) patients who had Y chromosome material. The karyotype in 7 of these patients did not suggest the presence of Y chromosome material. Seven of the patients had been ovariectomized before entering the study due to verified Y chromosome material, whereas three patients were operated upon after the DNA analysis. The histopathological evaluations showed that 1 of the 10 ovariectomized patients actually had a gonadoblastoma. The rest of the patients did not have gonadoblastoma or carcinoma in situ on histopathological evaluation. Three patients (age, >50 yr) positive for Y chromosome material chose not to have ovariectomy performed, and detailed ultrasonographies did not suggest the presence of gonadoblastoma. The frequency of Y chromosome material is high in Turner syndrome (12.2%), but the occurrence of gonadoblastoma among Y-positive patients seems to be low (7–10%), and the risk may have been overestimated in previous studies, perhaps due to problems with selection bias. This study emphasizes the need for prospective unbiased studies.


1992 ◽  
Vol 42 (6) ◽  
pp. 807-812 ◽  
Author(s):  
Patricia Y. Fechner ◽  
Kirby D. Smith ◽  
Ethylin Wang Jabs ◽  
Claude J. Migeon ◽  
Gary D. Berkovitz

2008 ◽  
Vol 14 (2) ◽  
pp. 83-89 ◽  
Author(s):  
M. Gaál ◽  
J. László ◽  
P. Bósze

1981 ◽  
Vol 58 (3) ◽  
pp. 282-284 ◽  
Author(s):  
G. Ponzio ◽  
M. DeMarchi ◽  
A. Carbonara ◽  
A. Godano ◽  
F. Massara

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