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Papillary Carcinoma Derived from Ovarian Mature Cystic Teratoma: A New Case Report and Literature Review

Case Reports in Clinical Medicine 2014年第4期3卷 197-202页

作者： Ihsane Souaf Hinde El Fatemi Amal Bennani Chbani Leila hammas nawale Harmouch Tawfik Afaf Amarti Department of Pathology Hassan II Teaching Hospital Fez Morocco

Introduction: Papillary carcinoma arising from thyroid tissue in mature cysticteratoma (MCT) of the ovary is extremely rare, and it is not easy to diagnose preoperatively. No clinical, no radiological, no biological signs are specific to malignant transformation. Case presentation: A 51-year-old woman had a left ovarian tumor measuring approximately 18 cm diameter with malignant transformation of a mature cysticteratoma, who was diagnosed postoperatively with follicular variant of papillary thyroid carcinoma. A laparoscopic hysterectomy and left salpingo-oophorectomy were performed. During surgery, there were no signs of invasion or metastasis. Conclusion: Consideration should be given to thyroidectomy followed by total-body scanning and serum studies for foci of thyroid carcinoma and adjuvant therapy with thyroidectomy and radio ablation if residual disease is identified.

关键词： Ovarian Teratoma Papillary Carcinoma Malignant Transformation Thyroid Ovarian Neoplasm

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Signet Ring Cell Carcinoma of Ampulla of Vater: Report of a Rare Malignancy and Literature Review

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Case Reports in Clinical Medicine 2014年第3期3卷 145-148页

作者： Ihsane Souaf Kawtar Znati Sanae Chahbouni Imane Hafid Hassania Ameurtesse nawale hammas Leila Chbani Hinde El Fatemi Tawfik Harmouch Afaf Amarti Department of Pathology Hassan II University Hospital of Fez Hassan Morocco

Introduction: Signet ring cell carcinoma is a rare tumor that generally originates in the gastrointestinal tract. Signet-ring cell carcinoma of the ampulla of Vater is extremely uncommon and a very rare clinical entity, which is infrequently reported in medical literature and only 31 cases have been mentioned. Most tumors affecting Vater’s Ampulla are adenocarcinomas and other histological variants are less frequent. It mainly occurs in elderly patients. Case Presentation: We report a case of signet ring cell carcinoma of Vater’s Ampulla. The tumour had infiltrated the duodenal, but local lymph nodes were clear (T3N0M0). Duodenopancreatectomy with pylorus preservation is the treatment of choice. Conclusions: Etiology and survival are not well-defined in the literature due to the extreme rarity of this disease.

关键词： Ampulla of Vater Carcinoma Signet Ring Cell Pancreas

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