PSEUDOPRECOCIOUS PUBERTY DUE TO A VERY SM ALL LEYDIG-CELL TUMOR - ENDOCRINOLOGIC INVESTIGATIONS, DIFFERENTIAL-DIAGNOSIS AND PROBLEMS OF IMAGING MODALITIES
W. Hoepffner et al., PSEUDOPRECOCIOUS PUBERTY DUE TO A VERY SM ALL LEYDIG-CELL TUMOR - ENDOCRINOLOGIC INVESTIGATIONS, DIFFERENTIAL-DIAGNOSIS AND PROBLEMS OF IMAGING MODALITIES, Monatsschrift fur Kinderheilkunde, 143(4), 1995, pp. 341-345
We report on a 8 2/12 year old boy with marked signs of precocious pub
erty (height 134.4 cm, pubic hair Tanner stage III, bone age 13 3/12 y
ears, mean serum testosterone concentration 6.6 nmol/l). The testicula
r volume was only 2 ml. After having excluded congenital adrenal hyper
plasia and true precocious puberty the differential diagnostic evaluat
ion had to take into account a tumor of the adrenals secreting androge
ns, a Leydig cell tumor, or a familial male limited precocious puberty
. Despite repeated investigations of the testes a testicular tumor was
revealed first only 14 month later. Histological examination showed a
Leydig cell tumor. It must be stated retrospectively that the sonogra
phic investigation which is of high diagnostic importance, needs a 7.5
MHz-scanner as a minimum to detect small testicular tumors. The MR Im
aging has a higher sensitivity but low specifity.