Clinical and laboratory observations were made in three children with isosexual precocity. None of the patients showed abnormalities in neurological or visual-field examinations although one patient had arrested hydrocephalus and a head circumference greater than the 98th percentile for her age and another patient had a history of seizures. Roentgenograms of the skull were normal in all patients. Cranial computerized tomography (CT) identified a lesion in each patient. We believe that craniel CT should be performed in any patient with isosexual precocity in whom a specific cause is not evident or in whom a cerebral cause is suggested even though the patient may be otherwise normal. Cranial CT is a safe, accurate, and noninvasive technique.
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http://dx.doi.org/10.1001/archpedi.1980.02130130017006 | DOI Listing |
Endocrinol Metab Clin North Am
June 2024
Division of Endocrinology, Children's National Hospital, 111 Michigan Avenue Northwest, Washington, DC 20010, USA.
Isolated vaginal bleeding before the onset of puberty is a rare presentation of isosexual precocity. In most cases, isolated vaginal bleeding without an abnormal genital examination is self-limited with resolution usually within 1 to 3 episodes. Watchful waiting is appropriate in most patients who do not have persistent bleeding, other signs of puberty, or signs/symptoms of an underlying etiology.
View Article and Find Full Text PDFJ Pak Med Assoc
December 2023
Department of Paediatric Endocrinology, National Institute of Child Health, Karachi, Pakistan.
A male child, aged seven months, visited the out patients clinic of the National Institute of Child Health, Karachi, in May 2020 with the features of iso-sexual puberty. After ruling out the more common causes of early puberty, like congenital adrenal hyperplasia and tumours secreting chorionic gonadotropin hormone, hormonal assessment indicated raised testosterone independent of gonadotropin. The volume of the testicles was symmetric and testicular ultrasonography revealed no mass.
View Article and Find Full Text PDFCureus
February 2022
Endocrinology and Diabetes, Nil Ratan Sircar Medical College, Kolkata, IND.
Juvenile granulosa cell tumor leading to isosexual peripheral precocious puberty is a well-known association. Here, we report a rare case of central precocious puberty secondary to granulosa cell tumor of the ovary. A five-year and five-month-old girl presented with a history of progressive enlargement of bilateral breasts and intermittent vaginal spotting, associated with growth acceleration.
View Article and Find Full Text PDFJ Pediatr Endocrinol Metab
June 2022
Department of Radiodiagnosis, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Objectives: Feminizing adrenal tumors are rare in childhood. We present a case of a special category of adrenal tumor, an oncocytoma, causing isosexual peripheral precocity.
Case Presentation: A 4-year old girl presented with breast development and menstrual bleeding over a period of 3-4 months.
Int J Gynecol Pathol
July 2021
Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
The common ovarian follicle cyst is typically straightforward from both clinical and pathologic perspectives, but may have a variety of unusual features from both aspects at various stages of life. Lack of familiarity with these may lead to diagnostic quandaries, the most common of which is distinguishing between a follicle cyst and cystic granulosa cell tumor of either adult or juvenile type. We reviewed 30 cases of follicle cysts, all sent in consultation, to highlight unusual aspects of a common lesion.
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