J Pathol Transl Med.  2015 May;49(3):262-266. 10.4132/jptm.2015.03.26.

Follicular Proliferative Lesion Arising in Struma Ovarii

Affiliations
  • 1Department of Pathology, Seoul National University College of Medicine, Seoul, Korea.
  • 2Department of Pathology, Hallym University College of Medicine, Seoul, Korea.
  • 3Department of Epidemiology and Preventive Medicine, Graduate School of Public Health, Seoul National University, Seoul, Korea. lilloa@snu.ac.kr

Abstract

Malignant struma ovarii is extremely rare and difficult to diagnose histologically, particularly in cases of follicular carcinoma. This case study is intended to describe three cases of follicular proliferative lesion arising in struma ovarii that we experienced. The first case was clearly malignant given the clinical picture of multiple recurrences, but there was little histological evidence of malignancy. Our second case featured architectural and cellular atypia and necrosis and was diagnosed as malignant despite the absence of vascular and stromal invasion. Our third case exhibited solid microfollicular proliferation without any definite evidence of malignancy (even the molecular data was negative); however, we could not completely exclude malignant potential after conducting a literature review. In cases such as our third case, it has been previously suggested that a diagnostic term recognizing the low-grade malignant potential, such as "proliferative stromal ovarii" or "follicular proliferative lesion arising in the stromal ovarii" would be appropriate.

Keyword

Follicular proliferative lesion; Adenocarcinoma, follicular; Malignant struma ovarii

MeSH Terms

Adenocarcinoma, Follicular
Necrosis
Recurrence
Struma Ovarii*

Figure

  • Fig. 1. Peritoneal nodules found intraoperatively (A) and the microscopic findings (B, C). HBME1 positivity of microfollicles of the first case (D) is observed and the initial ovarian lesion of the first case (E) shows vascular invasion (E, inset). The gross features of the second case (F) and the histological findings (G, H) are suggestive of malignancy, and HBME1 status is positive only in the cytoplasm (I). In the third case, the solid regions are tiny and scattered (J). Microscopically, microfollicles are predominant (K), and cyclin D1 expression is increased (L).


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