Two Cases of Malignant Struma Ovarii with Metastasis to Pelvic BoneSteinman R.A. · De Castro I.O. · Shrayyef M. · Chengazi V. · Giampoli E. · Van Der Sloot P. · Calvi L.M. · Wittlin S.D. · Hammes S.R. · Hou R.
aDivision of Endocrinology and Metabolism, Departments of bRadiology, and cPathology, dDivision of Otolaryngology, University of Rochester School of Medicine, Rochester, N.Y., USA; eDepartment of Medicine, Moncton Hospital, Moncton, N.B., fDepartment of Medicine, Dalhousie University, Halifax, N.S., and gDepartment of Medicine, Memorial University, St. John, Nfld., Canada
Histologically, malignant struma ovarii metastasizes rarely, and only a few cases reported bone metastasis. Here, we describe 2 cases of biologically malignant struma ovarii with pelvic bone metastasis. Case 1 is a 22-year-old female who was found to have a large left ovarian mass during routine prenatal ultrasound. Papillary thyroid cancer arising in struma ovarii was identified after laparoscopic salpingo-oophorectomy. After total thyroidectomy, radioactive iodine whole-body scan revealed extrathyroidal iodine uptake in left anterior pelvis. Subsequent I-131 treatment resolved the pelvic metastasis. Case 2 is a 49-year-old female who was diagnosed with malignant struma ovarii in 1996 and presented in 2007 with pelvic recurrence and extensive left hip metastasis. Treatment with resection of the pelvic tumor, total thyroidectomy, and multiple I-131 ablation led to eventual resolution of the abdominal and left hip foci. In conclusion, we present 2 rare cases of malignant struma ovarii, both with metastasis to the pelvic bone. This report makes pelvic bone the most frequent site for bone metastasis in malignant struma ovarii. It also emphasizes the importance of total thyroidectomy in allowing identification and treatment of bony metastasis with radioactive iodine.
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