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Precocious puberty secondary to massive ovarian oedema in a 6-month-old girl
Anuja Natarajan1, Jeremy K H Wales, Sean S Marven
1Department of Paediatric Endocrinology, Sheffield Children's Hospital, Western Bank, Sheffield S10 2TH, UK.
Insights
Massive ovarian edema, a rare condition, caused sexual precocity in a 6-month-old infant. This case highlights the need to consider ovarian abnormalities in pediatric sexual precocity.
Area of Science:
- Pediatric Endocrinology
- Reproductive Endocrinology
- Gynecologic Pathology
Background:
- Sexual precocity in infants requires thorough investigation to rule out serious underlying conditions.
- Adrenal and central causes are common considerations for precocious puberty.
Observation:
- A 6-month-old female presented with premature thelarche and pubarche.
- Ultrasound revealed enlarged ovaries with mixed solid and cystic components.
- Clinical progression of precocious puberty was noted.
Findings:
- Laparotomy excluded neoplasia.
- Histopathology confirmed massive ovarian edema (MOE).
- MOE was identified as the cause of sexual precocity in this infant.
Implications:
- Massive ovarian edema is an underrecognized cause of sexual precocity in young children.
- This case emphasizes the importance of considering MOE in the differential diagnosis of pediatric precocious puberty.
- Early recognition and appropriate management are crucial for favorable outcomes.
Abstract:
A 6-month-old girl was referred with breast and pubic hair development. Investigations excluded an adrenal or central cause for her precocity. Ovarian ultrasound scans showed bilaterally enlarged ovaries with both solid and cystic changes. A follow-up examination suggested progression of the precocity and in view of the young age of the child, and concerns regarding underlying malignancy, she underwent laparotomy. Histology showed no evidence of neoplasia but there was stromal oedema consistent with a diagnosis of massive ovarian oedema. This entity is poorly recognised in the paediatric literature as a cause of sexual precocity, and has never previously been described in such a young patient. This is an unusual cause of precocity in a young child and its recognition and management are reviewed.
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