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A Rare Case of Adenoid Cystic Carcinoma of the Breast: Discussion and Review of the Literature

Case Reports in Clinical Medicine 2014年第7期3卷 433-436页

作者： saad lannaz Imane Ouziane Youssef Bensouda Hind Mrabti Hassan Errihani Department of Medical Oncology National Institute of Oncology Rabat Morocco

Adenoid cystic carcinoma (ACC) of the breast is a rare type of primary breast cancer with a favorable prognosis, despite its triple-negative status. There has been no consensus regarding treatments. We will report a case of Adenoid cystic carcinoma of the breast presented with localized disease and no axillary lymph node metastases. We performed a radical mastectomy with axillary lymph node dissection, with a favorable clinical course and we will describe the clinic pathologic features of ACC of the breast and review the current literature.

关键词： Adenoid Cystic Carcinoma Triple-Negative Breast Carcinoma

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Peripheral Primary Neuroectodermal Tumour of the Ileum: A Case Report and Review of the Literature

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Journal of Cancer Therapy 2021年第7期12卷 399-408页

作者： Soukaina Harrak Siham Lemsanes Sawsan Razine Salma Najem Khadija Benchekroun saad lannaz Hind Mrabti Hassan Errihani Department of Medical Oncology National Institute of Oncology Rabat Morocco

Background: Ewing’s Sarcoma (ES)/peripheral Primitive Neuroectodermal Tumor (pPNET) is a rare aggressive malignant small round cell tumour. Most of them arise in bony sites, and they represent the second commonest primary osseous malignancy in adolescence and young adults. The localization of the small bowel is very rare, to our knowledge only 35 cases of ES/pPNET of the small bowel have been reported in the literature. Case Presentation: We report a case of pPNET of the ileum in a 26-year-old female, presented abdominal pain with a transit disorder. The clinical examination was unremarkable. The histological and immunohistochemical study confirmed the diagnosis of peripheral primary neuroectodermal tumours. The patient was treated by tumor resection followed by adjuvant chemotherapy. The evolution was good, without recurrence with a follow-up of 12 months. Conclusion: PNET of the ileum is very rare. We report this case to enrich the database of this rare clinical entity and to improve the management of patients with PNET of the ileum.

关键词： Ewing’s Sarcoma Primitive Neuroectodermal Tumor Small Bowel Sarcoma Extraosseous Sarcoma

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