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Papillary Thyroid Carcinoma in Struma Ovarii.
Pooja Devi1, Maryam Aghighi1, Nagy Mikhail2
1Pathology, Saint Barnabas Medical Center, Robert Wood Johnson Barnabas Health, Livingston, USA.
Cureus
|May 12, 2020
Summary
Struma ovarii, a rare germ cell tumor, can present as a pelvic mass. This case highlights a rare malignant variant with papillary thyroid carcinoma features.
Area of Science:
- Gynecologic Oncology
- Endocrinology
- Pathology
Background:
- Struma ovarii is a rare germ cell tumor predominantly composed of thyroid tissue, typically unilateral.
- Malignancy arising in struma ovarii is exceptionally uncommon.
- Pelvic masses in peri- and postmenopausal patients warrant a broad differential diagnosis.
Observation:
- A case of struma ovarii presenting as abdominal distension in a female patient.
- Surgical management involved total hysterectomy and bilateral salpingo-oophorectomy.
- Histopathology revealed mature thyroid follicles and a focal area with nuclear features of papillary thyroid carcinoma.
Findings:
- The diagnosis was struma ovarii with focal papillary thyroid carcinoma.
- No other teratomatous elements were identified in the resected specimen.
- Patient's thyroid hormone levels were within normal ranges.
Implications:
- Struma ovarii should be considered in the differential diagnosis of ovarian masses.
- This case underscores the rare possibility of malignant transformation within struma ovarii.
- Early recognition and appropriate surgical management are crucial for favorable outcomes.
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