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34 results on '"Fatemi, H"'

19. Tumeur plantaire

Author

Bounouar, M., Meziane, M., El Bakkal, A., Mikou, O., Mernissi, F., Belghiti, H., El Fatemi, H., Harmouch, T., and Amarti, A.

Published
2011
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21. [Urothelial carcinoma involving the renal calyce revealed due to brain metastasis].

Author

Mustapha A, Shamalirwa BB, Wembonyama JPO, Tidahy R, Boubacar E, El Fatemi H, Soufiane M, Fadl TM, and Hassan FM

Subjects
Aged, Brain Neoplasms diagnosis, Female, Hematuria etiology, Humans, Kidney Neoplasms pathology, Kidney Neoplasms secondary, Brain Neoplasms pathology, Kidney Calices pathology, Kidney Neoplasms diagnosis
Abstract

Urothelial carcinoma is usually characterized by severe symptoms including macroscopic haematuria. We here report the case of a female patient without a history of smoking or urothelial carcinoma, making it, to our knowledge, a unique case and a first case of urothelial carcinoma revealed by brain metastasis., Competing Interests: Les auteurs ne déclarent aucun conflit d'intérêts., (© Ahsaini Mustapha et al.)

Published
2019
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22. [Pleural epithelioid sarcoma: about a case and review of the literature].

Author

Ouahbi H, Akasbi Y, Oualla K, Amara B, Chatar A, Tizniti S, Fatemi H, Lemrabet FZ, Arifi S, and Mellas N

Subjects
Adult, Doxorubicin administration & dosage, Fatal Outcome, Female, Humans, Ifosfamide administration & dosage, Neoplasm Metastasis, Pleural Neoplasms drug therapy, Sarcoma drug therapy, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Pleural Neoplasms pathology, Sarcoma pathology
Abstract

Proximal epithelioid sarcoma (PES) originating from the pleura is a clinical entity rarely reported in the literature. We report the case of a young patient with immediately metastatic proximal epithelioid sarcoma (PES) treated at the Department of Medical Oncology, Fes. Treatment consisted of chemotherapy based on doxorubicin and ifosfamide. After the first cycle of chemotherapy, the disease led to a fatal outcome. Our case study highlights the potentially aggressive behaviour of PES which represents a clinical trap and can be life-threatening., Competing Interests: Les auteurs ne déclarent aucun conflit d'intérêts.

Published
2016
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24. [Dermatofibrosarcoma protuberans : report of 27 cases and review of the literature].

Author

Hammas N, Badioui I, Znati K, Benlemlih A, Chbani L, El Fatemi H, Harmouch T, Bouyahyaoui Y, Boutayeb F, Mrini A, Mesbahi O, Mernissi FZ, and Amarti A

Subjects
Adolescent, Adult, Aged, Antigens, CD metabolism, Antigens, CD34 metabolism, Antigens, Differentiation, Myelomonocytic metabolism, Biomarkers, Tumor metabolism, Calmodulin-Binding Proteins metabolism, Combined Modality Therapy, Dermatofibrosarcoma metabolism, Dermatofibrosarcoma therapy, Desmin metabolism, Female, Humans, Male, Middle Aged, Retrospective Studies, Skin Neoplasms metabolism, Skin Neoplasms therapy, Young Adult, Dermatofibrosarcoma pathology, Skin Neoplasms pathology
Published
2014
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25. [The primary melanoma of the female genital tract: report of three cases and review of literature].

Author

Bennani A, el Fatemi H, Erraghay S, Mobakir H, Ameurtess H, Souuaf I, Moumna K, Idrissi K, Zriouel A, Squalli N, Banani A, and Amarti A

Subjects
Adult, Female, Humans, Melanoma epidemiology, Melanoma therapy, Uterine Cervical Neoplasms epidemiology, Uterine Cervical Neoplasms therapy, Vaginal Neoplasms epidemiology, Vaginal Neoplasms therapy, Melanoma diagnosis, Uterine Cervical Neoplasms diagnosis, Vaginal Neoplasms diagnosis
Published
2013
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26. [Breast metastases of gastric adenocarcinoma associated with a pregnancy of 32 weeks of gestation: about a rare case].

Author

Jayi S, Fatemi H, Laabadi K, Bouguern H, Chaara H, Laamarti A, and Melhouf MA

Subjects
Adenocarcinoma diagnosis, Adult, Breast Neoplasms diagnosis, Female, Humans, Pregnancy, Pregnancy Trimester, Third, Stomach Neoplasms diagnosis, Adenocarcinoma pathology, Breast Neoplasms secondary, Pregnancy Complications, Neoplastic diagnosis, Stomach Neoplasms pathology
Published
2013
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29. [The search for protein overexpression and HER2 gene amplification in gastric cancer by immunohistochemistry and in situ hybridization: experience of the CHU Hassan II of Fez].

Author

El Fatemi H, Hammas N, Idrissi K, Mellas N, Bennani A, Amarti A, Cayre A, Penault-llorca F, and Mesbahi O

Subjects
Adenocarcinoma pathology, Adult, Aged, Aged, 80 and over, Female, Gene Amplification, Humans, Immunohistochemistry, In Situ Hybridization, Fluorescence, Male, Middle Aged, Stomach Neoplasms pathology, Young Adult, Adenocarcinoma genetics, Gene Expression Regulation, Neoplastic, Genes, erbB-2 genetics, Stomach Neoplasms genetics
Published
2012

30. [Neuroendocrine carcinoma of the breast: about a case and review of the literature].

Author

El Fatemi H, Hammas N, Moumna K, Bedahou M, Mellas N, and Mesbahi O

Subjects
Breast Neoplasms epidemiology, Breast Neoplasms metabolism, Breast Neoplasms pathology, Carcinoma, Neuroendocrine epidemiology, Carcinoma, Neuroendocrine metabolism, Carcinoma, Neuroendocrine pathology, Female, Humans, Immunohistochemistry, Middle Aged, Breast Neoplasms diagnosis, Carcinoma, Neuroendocrine diagnosis
Published
2012

31. [Association pregnancy and pseudomyxoma peritonei secondary to mucinous borderline tumor of the ovary: about a case and review of the literature].

Author

Jayi S, Fatemi H, Bouguern H, Chaara H, and Melhouf MA

Subjects
Adenocarcinoma, Mucinous complications, Adenocarcinoma, Mucinous diagnosis, Adult, Female, Humans, Ovarian Neoplasms complications, Ovarian Neoplasms diagnosis, Peritoneal Neoplasms diagnosis, Pregnancy, Pseudomyxoma Peritonei diagnosis, Adenocarcinoma, Mucinous pathology, Ovarian Neoplasms pathology, Peritoneal Neoplasms secondary, Pregnancy Complications, Neoplastic diagnosis, Pseudomyxoma Peritonei etiology
Published
2012

32. [Buschke-Lowenstein tumor associated with scrotal melanoma. A case report].

Author

Chraïbi M, Harmouch T, Znati K, El Fatemi H, Chbani L, Bennis S, Amarti A, Ahallal Y, and Farih MH

Subjects
Aged, Buschke-Lowenstein Tumor, Condylomata Acuminata surgery, Genital Neoplasms, Male surgery, Humans, Male, Melanoma surgery, Penile Neoplasms surgery, Scrotum surgery, Condylomata Acuminata pathology, Genital Neoplasms, Male pathology, Melanoma pathology, Penile Neoplasms pathology, Scrotum pathology
Abstract

Buschke-Lowenstein tumour (BLT) is a giant condyloma acumina, which is rare entity and represents only 1% of all populace. It is a rare viral disease, essentially transmitted by sexual intercourse, characterized by a potential for malignant transformation, invasion and recurrence after treatment. We report a case of BLT associated with perinea-scrotal melanoma. This association was never described in the literature. The purpose of our case report is to discuss the clinical and pathological appearances of these two entities and to outline the recent studies of molecular biology, which can explain this association., (Copyright © 2011. Published by Elsevier Masson SAS.)

Published
2012
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33. [Plantar tumor].

Author

Bounouar M, Meziane M, El Bakkal A, Mikou O, Mernissi F, Belghiti H, El Fatemi H, Harmouch T, and Amarti A

Subjects
Adult, Female, Humans, Foot Dermatoses pathology, Warts pathology
Published
2011
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34. [Femoral metaphyso-diaphyseal chondroblastoma: a case report].

Author

Znati K, Ahaouch M, Fatemi H, Chbani L, Affifi A, Kamaoui I, Bennis S, and Amarti A

Subjects
Adolescent, Biopsy, Diagnosis, Differential, Diaphyses pathology, Female, Humans, Immunohistochemistry, Phosphopyruvate Hydratase analysis, S100 Proteins analysis, Vimentin analysis, Chondroblastoma diagnosis, Femoral Neoplasms diagnosis
Abstract

Chondroblastoma is a rare benign tumor of cartilage tissue accounting for less than 1% of all bone tumors. The epiphysis of long bones is the typical localization, often extending to the metaphysis. Metaphyseal, metaphysodiaphyseal or pure diaphyseal forms are exceptional. We report a case in a 15-year-old boy who presented a metaphyso-diaphyseal chondroblastoma of the distal portion of the left femur. The inaugural signs were pain and limited joint motion. We discuss the anatomic aspects and the clinical course of this rare tumor and present current knowledge of the histogenesis.

Published
2007
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