| Literature DB >> 31149505 |
Yoko Furutake1, Tomoyuki Fukagawa1, Yasuko Suga1, Takayuki Nagasawa1, Seiya Sato1, Hideo Omi1, Masahiro Kagabu1, Atsumi Chiba1, Tadahiro Shoji1, Satoshi Takeuchi1, Tamotsu Sugai2, Hiroaki Itamochi1, Toru Sugiyama1.
Abstract
Primary ovarian leiomyosarcoma (POLMS) is extremely rare, and optimal therapy for this disease is unknown. A 40-year-old woman presented at a local hospital with abdominal pain. Tumor resection of the left ovary was performed. The pathological diagnosis was leiomyoma of the left ovary. Nine months after surgery, she developed of severe back pain and a subcutaneous tumor on her left shoulder. Magnetic resonance imaging and computed tomography revealed left ovarian tumor recurrence, pelvic bone metastasis, and multiple liver masses. Biopsy of the subcutaneous tumor on her left shoulder demonstrated metastatic leiomyosarcoma. The previously resected left ovarian tumor was re-examined, and the tumor was found to be a leiomyosarcoma. The patient received gemcitabine 800 mg/m2 and docetaxel 60 mg/m2 (GD therapy), administered at 3-week intervals. After three cycles of GD therapy, the patient experienced dyspnea and was diagnosed with mild interstitial pneumonia. Oral corticosteroid therapy resulted in complete symptom improvement. Thereafter, the dosage of GD was decreased, and after 13 cycles of GD therapy, radiofrequency ablation was performed twice for liver metastases. The tumors have shrunk by 65.5% after 23 cycles of GD. She remains alive after undergoing 24 cycles of GD. GD therapy may be effective for POLMS.Entities:
Keywords: Chemotherapy; Docetaxel; Gemcitabine; Leiomyosarcoma; Ovary; Radiofrequency ablation
Year: 2017 PMID: 31149505 PMCID: PMC6498255 DOI: 10.1007/s13691-017-0309-7
Source DB: PubMed Journal: Int Cancer Conf J ISSN: 2192-3183