Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Khadija Benhayoune"'
Autor:
Khadija Benhayoune, Hinde El Fatemi, Meryem El Ghaouti, Abdelaziz Bannani, Abdelilah Melhouf, Taoufik Harmouch
Publikováno v:
The Pan African Medical Journal, Vol 20, Iss 124 (2015)
Vaginal metastasis from pancreatic cancer is an extreme case and often indicates a poor prognosis. We present a case of pancreatic carcinoma with metastasis to the vagina that was discovered by vaginal bleeding. To our knowledge, this is the third ca
Externí odkaz:
https://doaj.org/article/2ab030674d714a1cb4931611c50ad7f5
Publikováno v:
The Pan African Medical Journal, Vol 20, Iss 77 (2015)
Adenoid cystic carcinoma of the cervix is a rare and aggressive tumor with fatal outcome. In this paper we report two cases of primary adenoid cystic carcinoma and a review of literature. A 80 years old woman, admitted to our hospital with postmenopa
Externí odkaz:
https://doaj.org/article/d6cce78d87ab48f390ed0a158ecedba5
Autor:
Lamiae Boudahna, Zineb Benbrahim, Lamiae Amaadour, Aicha Mazouz, Khadija Benhayoune, Yassir Tahiri, Moulay Hassan Farih, Afaf Amarti, Samia Arifi, Nawfel Mellas
Publikováno v:
The Pan African Medical Journal, Vol 19, Iss 279 (2014)
Paratesticular embryonal rhabdomyosarcoma (RMS) is a rare tumor arising from the mesenchymal tissues of the spermatic cord, epididymis, testis and testicular tunics. We report three cases of adult paratesticular RMS, two embryonic and one pleomorphic
Externí odkaz:
https://doaj.org/article/d2c2c5d2b08d47c3b924ec01e2c0dac7
Autor:
Taoufiq Harmouch, Khadija Benhayoune, Hinde El Fatemi, Soufiane Mellas, Jamal Mohammed El Fassi, Nawal Hammas, H. Farih, Laila Chbani
Publikováno v:
Case Reports in Clinical Medicine. :93-96
Cutaneous metastasis from renal cell carcinoma is believed to be rare. We present a 66-year-old man operated for kidney cancer 20 years ago and has consulted for a scrotal lesion that had started 20 days. The physical examination revealed an erythema
Autor:
Mohammed El Merini, Hassan El Fettach, Khadija Benhayoune, Taoufik Harmouch, Faouzi Boutayeb, Siham Tizniti, Hinde El Fatemi
Publikováno v:
Case Reports in Clinical Medicine. :644-649
Introduction: Soft tissue chondroma is a very rare, slow progressing, benign tumor. It has a specific tendency for hands and feet. It can exhibit worrisome radiographic and histologic features mimicking chondrosarcomas. Case 1: A 54-year-old man was
Autor:
Khadija Benhayoune, Zineb Benbrahim, Layla Chbani, Samia Arifi, Nawfel Mellas, Lamiae Amaadour
Publikováno v:
Journal of Cancer Therapy. :1000-1004
Aggressive fibromatosis arising from the small bowel mesentery is extremely rare. It may occur in association with previous trauma, abdominal surgery, drugs, Gardner’s syndrome, or familial adenomatous polyposis. This paper presents a 32-year-old m
Autor:
Taoufik Harmouch, Abdelilah Melhouf, Khadija Benhayoune, Hinde El Fatemi, Abdelaziz Bannani, Meryem El Ghaouti
Publikováno v:
The Pan African Medical Journal
The Pan African Medical Journal, Vol 20, Iss 124 (2015)
Pan African Medical Journal; Vol 20, No 1 (2015)
The Pan African Medical Journal, Vol 20, Iss 124 (2015)
Pan African Medical Journal; Vol 20, No 1 (2015)
Vaginal metastasis from pancreatic cancer is an extreme case and often indicates a poor prognosis. We present a case of pancreatic carcinoma with metastasis to the vagina that was discovered by vaginal bleeding. To our knowledge, this is the third ca
Publikováno v:
The Pan African Medical Journal
The Pan African Medical Journal, Vol 20, Iss 77 (2015)
The Pan African Medical Journal, Vol 20, Iss 77 (2015)
Adenoid cystic carcinoma of the cervix is a rare and aggressive tumor with fatal outcome. In this paper we report two cases of primary adenoid cystic carcinoma and a review of literature. A 80 years old woman, admitted to our hospital with postmenopa
Autor:
Khadija Benhayoune, Jalal Eddine Elammari, Abdelhak Khallouk, Mohammed Jamal El Fassi, Rajae Kanab, Youssef Kharbach, Soufiane Mellas, My Hassan Farih, Ahmed Amine Bouchikhi, Mohammed Fadl Tazi, Karim Lahlaidi
Publikováno v:
Journal of Medical Case Reports
Introduction An embryonic paratesticular rhabdomyosarcoma is a very rare mesenchymal tumor. It is an intrascrotal tumor that is localized in paratesticular structures such as the epididymis or spermatic cord. Rhabdomyosarcoma is most often observed i