cover
Article Per Year (5 Year)
All
Home Page
OAI Link
Editorial Team
Contact
Reviewer
Google Scholar
Contact Name
-
Contact Email
-
Phone
-
Journal Mail Official
-
Editorial Address
-
Location
,
INDONESIA
Journal of Medical Biomedical and Applied Sciences
Published by Innovative Journal
ISSN : -     EISSN : -     DOI : -
Core Subject : Health, Science,
Biochemistry, Genetics & Molecular Biology Medicine & Pharmacology
Arjuna Subject : -
Articles 3 Documents
 1 
Search results for , issue " Vol 6 No 12 (2018)" : 3 Documents clear
OCT-angiography is inappropriate to demonstrate causality of peripapillary hypodensity in LHON Finsterer, MD, PhD, Josef
Journal of Medical Biomedical and Applied Sciences Vol 6 No 12 (2018)
Publisher : Journal of Medical Biomedical and Applied Sciences

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (78.994 KB) | DOI: 10.15520/jmbas.v6i12.171

Abstract

see the full pdf
UTERINE LEIOMYOSARCOMA: About 13 Cases and Review of the Literature FZ, TERRAB; F., ALLOUCH; S., GHAMAD; T., BOUHAFA; Z., ALAMI; K., HASSOUNI
Journal of Medical Biomedical and Applied Sciences Vol 6 No 12 (2018)
Publisher : Journal of Medical Biomedical and Applied Sciences

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (116.033 KB) | DOI: 10.15520/jmbas.v6i12.172

Abstract

The uterine leiomyosarcoma (LMS) is a rare cancer arising from the smooth myometrial cells. The LMS is clinicallyaggressive malignancy, accounting for 2% to 6% of uterine malignancies and a very low annual incidence.Object of the study: To evaluate management and outcome of the treatment of uterine leiomyosarcoma.Patients and methods: Retrospective study of a series of 13 patients treated for uterine leiomyosarcoma in thedepartment of radiotherapy of CHU Hassan II, Fes between 2012 and 2016Results: The condition is rarely suspected preoperatively, diagnosis is usually made on histological examination ofthe operative specimen. The outcome is related to the mitotic activity of the tumour and to the infiltration of nearlystructures. Surgery is the only effective treatment, chemotherapy is ineffective, adjuvant radiotherapy improves localcontrol of the tumour but has no incidence on survival.Conclusion: In the absence of an effective adjuvant treatment, uterine leiomyosarcoma bears a poor prognosis withthe only exception of small non infiltring tumours with a low mitotic activity.
Hodgkin’s disease in children: Experience of Radio-therapy Department CHU HASSAN II Fez GHAMMAD, S.; ALLOUCHE, F.; TERRAB, FZ.; HASSANI, G. CHEBIHI; BOUHAFA, T.; ALAMI, Z.; HASSOUNI, K.
Journal of Medical Biomedical and Applied Sciences Vol 6 No 12 (2018)
Publisher : Journal of Medical Biomedical and Applied Sciences

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1002.719 KB) | DOI: 10.15520/jmbas.v6i12.173

Abstract

Hodgkin lymphoma is a type of malignant disorder in which Reed-Sterberg cells are present in a characteristicbackground of reactive inflammatory cells of various types, accompanied by fibrosis of variable degree.More than sixty years ago Hodgkin’s Lymphoma was considered a “systemic” malignancy and universally fatal. Morerecently less extensive radiation therapy in combination with chemotherapy has resulted in an excellent overall survivaland prolonged disease free survival in children.There is age specific difference in the representation of the various subtypes of Hodgkin lymphoma (lymphocyticpredominance 2–7% in adults and only 20% in children).

Page 1 of 1 | Total Record : 3

 1 

Filter by Year

2018 2018


Reset
Filter By Issues
All Issue Vol 7 No 2 (2019) Vol 7 No 1 (2019) Vol 6 No 12 (2018) Vol 6 No 11 (2018) Vol 6 No 10 (2018) Vol 6 No 9 (2018) Vol 6 No 8 (2018) Vol 6 No 7 (2018) Vol 6 No 6 (2018) Vol 6 No 5 (2018) Vol 6 No 4 (2018) Vol 6 No 3 (2018) Vol 6 No 2 (2018) Vol 6 No 1 (2018) Vol 5 No 12 (2017) Vol 5 No 10 (2017) Vol 5 No 08 (2017) Vol 5 No 07 (2017) Vol 5 No 06 (2017) Vol 5 No 04 (2017) Vol 5 No 9 (2017) Vol 5 No 3 (2017) Vol 5 No 2 (2017) Vol 5 No 1 (2017) Vol 3 No 12 (2016) Vol 4 (2016) Vol 3 (2016) Vol 1 (2014) More Issue