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Cystic struma ovarii: imaging findings
1Department of Radiology, Nippon Medical School, Chiba-Hokuso Hospital, Chiba, Japan. okada@nms.ac.jp
Journal of Computer Assisted Tomography
|June 23, 2000
Summary
This study presents three cases of cystic struma ovarii, a rare ovarian tumor. Even when completely cystic, struma ovarii should be considered in ovarian mass diagnoses.
Area of Science:
- Gynecologic pathology
- Ovarian neoplasms
- Endocrine pathology
Background:
- Struma ovarii is a rare germ cell tumor composed of thyroid tissue.
- It is typically found within an ovarian teratoma, often with a solid component.
- Completely cystic struma ovarii is exceptionally rare, posing diagnostic challenges.
Observation:
- The study details three cases of cystic struma ovarii lacking solid components.
- One case presented as a unilocular cystic mass with thin walls.
- Two cases were multilocular cystic masses, with specific MRI signal characteristics noted (T2 signal void, T1 intermediate intensity).
Findings:
- Preoperative diagnosis of cystic struma ovarii was challenging in all reported cases.
- The absence of a solid component can obscure the diagnosis.
- Characteristic MRI findings were observed in multilocular cystic variants.
Implications:
- Cystic struma ovarii must be included in the differential diagnosis of cystic ovarian masses.
- Radiological and pathological evaluation is crucial for accurate diagnosis.
- Awareness of this rare entity can improve patient management and outcomes.