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Feb 2019 DOI 10.14302/issn.2572-3030.jcgb-19-2581
Ashraf KhanCorresponding author
We report the case of a 75 year-old female with past history of ampullary adenocarcinoma presenting with a rapidly enlarging breast mass, initially misclassified on fine needle aspiration as a probable sarcoma, which was ultimately diagnosed as melanoma on resection in the absence of a known cutaneo…
Feb 2019 DOI 10.14302/issn.2689-5773.jcdp-19-2611
Cameron Y. S. LeeCorresponding author
An anatomical variant of the Stafne bone cavity (SBC) located in the right subcondylar region of the mandible is presented. Such an occurrence of the SBC in this region near the parotid gland is considered rare and poses a diagnostic challenge for the dentist and radiologist. Knowledge of head and n…
Aug 2018 DOI 10.14302/issn.2377-2549.jndc-18-2187
Elias RandjbaranCorresponding author
Among the numerous potential uses of carbon nanotubes (CNT), its utilization to fortify polymers was given careful consideration. This reason can be because of the remarkable firmness, magnificent quality, and the low thickness of CNT. This has given various chances to the innovation of new material…
Mar 2018 DOI 10.14302/issn.2639-1716.jn-18-1993
W. Kurtis ChildersCorresponding author
Cardiovascular disease and lung cancer are two of the most common causes of death in the United States. The cardioprotective benefits of statin class drugs is predominantly mediated through the inhibition of 3-hydroxy-3-methylglutaryl CoA (HMG-CoA) reductase, decreasing available mevalonate, and thu…
Jan 2018
Ala’a SharafCorresponding author
Ileal conduit has been considered the urinary diversion of choice following radical cystectomy although orthotopic bladder substitution is gaining popularity. Urinary diversions are associated with complications including stone formation in up to 54%. We report the management of the largest ileal co…
Dec 2017 DOI 10.14302/issn.2641-9181.ijnr-17-1859
Mohammad VaseiCorresponding author
Pericentric inversions in chromosome 10 are regarded as both common and rare conditions, based on breakage and rearrangement within each specific segment. We present phenotypic and cytogenetic characterizations of a rare recombinant chromosome 10, namely inv(10)(p11q26), in a 13-month-old flabby gir…
Nov 2017 DOI 10.14302/issn.2574-4526.jddd-17-1792
Anastasios AngelouCorresponding author
Objectives: Bariatric surgery has been established as the cornerstone of treatment of morbid obesity with good immediate and long-term results. Nutrient deficiencies though, can be an important long-term complication and may lead to hematological, metabolic and especially neurological disorders whic…
Nov 2017 DOI 10.14302/issn.2574-4518.jsdr-17-1754
Karim SedkyCorresponding author
Objective: Individuals diagnosed with Down syndrome (DS) are predisposed to obstructive sleep apnea (OSA). The aim of this study is to assess the prevalence of OSA and factors associated with OSA in this population. Study Design: Systematic literature review and meta-analysis. Methods: Studies of DS…
Nov 2016 DOI 10.14302/issn.2574-4526.jddd-16-1322
Mohammed DarouichiCorresponding author
Institute medical radiology
Summary Primary malignant melanoma arising from the parotid gland is extremely rare and only sporadic cases have been described. This entity is characterized by delayed diagnosis, poor prognosis and controversial pathogenesis. We report a case of primary malignant melanoma of the parotid gland in a…
Nov 2016 DOI 10.14302/issn.2574-4526.jddd-16-1311
M DarouichiCorresponding author
Department of radiology
Adenosquamous carcinoma of the stomach (ASCS) is extremely rare with less than one hundred cases published in the world literature. It is defined by combined adenocarcima and squamous cells carcinoma of the stomach. ASCS is clinically aggressive and has a poor prognosis, even when discovered at an e…
Sep 2016 DOI 10.14302/issn.2473-1005.jdoi-16-1137
Surena VahabiCorresponding author
EVC syndrome is a rare autosomal recessive genetic syndrome which its exact prevalence is unknown. The main manifestations of EVC include condro-ectodermal dysplasia, polydactyly, congenital heart defects and tooth and nail hypoplasia, and the survival rate of patients depends on the heart disease.…
Jun 2016 DOI 10.14302/issn.2574-4518.jsdr-16-1002
Carlo LovatiCorresponding author
University of Milan, Milan, Italy
Obstructive sleep apnea (OSA) syndrome is a common disease characterized by partial or complete collapse of the upper airway during sleep secondary to functional or anatomical factors. The gold standard method for OSA diagnosis is an overnight polysomnogram demonstrating repetitive obstructive apnea…
Dec 2015 DOI 10.14302/issn.2470-5020.jnrt-15-774
Kisito Kouassi Jean Marie QuenumCorresponding author
Calcified and Infected Hydatid Cysts Case Report and Literature Review
Jul 2015 DOI 10.14302/issn.2372-6601.jhor-15-657
Alvaro AguayoCorresponding author
Syndrome of inappropriate antidiuretic hormone secretion (SIADH) is a known side effect of several oncology drugs, but it is rarely seen secondary to vinblastine with only a few cases reported worldwide. Herein we present a patient with nodular lymphocyte-predominant Hodgkin disease that developed a…
Jun 2015 DOI 10.14302/issn.2379-8572.joa-14-548
Pang AaronCorresponding author
This article has been retracted on 25 March 2016. VIEW THE RETRACTION NOTICE (https://doi.org/10.14302/issn.2379-8572.joa-25-5867) Fibrous dysplasia is a rare disorder of bone that is uncommon in the head and neck region. Herein, we present a rare case of polyostotic fibrous dysplasia involving the…
Jun 2015 DOI 10.14302/issn.2379-8572.joa-25-5867
Pang AaronCorresponding author
May 2015 DOI 10.14302/issn.2574-4496.jtc-13-347
Emilio MevioCorresponding author
Primary thyroid leiomyosarcoma, is extremely rare, with only 19 cases reported in the literature to date. Onset of the tumor, which usually develops in only one lobe of the thyroid, is sudden and the tumor spreads rapidly to surrounding tissues. Preoperative differential diagnosis is extremely diffi…
Aug 2014 DOI 10.14302/issn.2576-182X.jbsc-13-348
AG RuggeriCorresponding author
Department of Neurology e Psichiatry, Division of Neurosurgery, Policlinico Umberto I, “La Sapienza” Università di Roma
Melanocytoma is a rare benign lesion arising from leptomeningeal melanocytes. Meningeal melanocytomas are commonly seen in the thoracic region of the spinal canal and may also arise in the cervical or lumbar region, most often located in the intradural extramedullary compartment 1. To our knowledge,…
Jun 2014 DOI 10.14302/issn.2372-6601.jhor-14-378
Monika Kulma-KreftCorresponding author
Progressive multifocal leukoencephalopathy (PML) is a rare complication associated, inter alia, with rituximab-based lymphoma treatment. PML diagnosis is made easier with the criteria recently published by the American Academy of Neurology. Unambiguous diagnosis of PML can be achieved by demonstrati…
Nov 2013 DOI 10.14302/issn.2324-7339.jcrhap-13-304
Alexandria Garavaglia WilsonCorresponding author
Antiretrovirals have traditionally been associated with much toxicity. Newer antiretrovirals are considered much less toxic relative to older antiretrovirals. Upon its FDA-approval in 2009, raltegravir’s adverse drug reaction profile was found to be similar to placebo. However, recently there have b…