ClinMed International Library

The ClinMed International Library is a repository and an open access publisher for medical research that covers a wide range of areas in Clinical Medicine. ClinMed serves as a global platform for medical practitioners and research scholars to foster their learning and professional acumen through an extensive portfolio of research articles and publications that can be accessed without any restrictions.

Dedicated to clinical medical research, we now publish over 70 quality peer-reviewed journals making all the articles freely accessible. The manuscripts submitted to ClinMed will be processed through standard parameters and international peer review systems. This has enabled us to establish new milestones in the global research arena in terms of cogency and integrity, and to disseminate highly credible and accredited research content for researchers, scholars, and practitioners across the globe.

We ensure that all researchers and authors publishing their papers with us retain copyrights, licensed under Creative Commons Attribution License that permits the unrestricted use and re-use of the content with proper citation.



  Last Updated: October 18, 2020

ClinMed Archive

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Articles Published

All articles are fully peer reviewed, free to access and can be downloaded from our ClinMed archive.

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 Open Access DOI:10.23937/2643-4512/1710050

Pathophysiology and Non-Pharmacological Management of Allergic Rhinitis

Kamlesh Kumar Dubey and Mila Nu Nu Htay

Article Type: Review Article | First Published: September 30, 2020

Allergic rhinitis (AR) is one of the commonest allergic manifestations affecting approximately 400 million people worldwide. It is associated with a reduced quality of life, low productivity in the workplace, and poor school performance. On the other hand, medical cost increases. Allergic rhinitis has a considerable effect on the quality of life and can have significant consequences if left untreated. Many patients downplay rhinitis symptoms as an inconvenience rather than a disease. The majorit...

 Open Access DOI:10.23937/2378-3656/1410322

Mesothelial Cells in Lymph Nodes Associated with Massive Pericardial and Bilateral Pleural Effusion, a Diagnostic Dilemma: Report of a Case

Mohammadali Boroumand, MD, Mina Ghorbanpour Landy, MD and Narges Shahbazi, MD

Article Type: Case Report | First Published: October 07, 2020

Malignant pleural mesothelioma is a rare neoplasm that mostly occurs in elderly men. Recurrent unilateral pleural effusion is the most typical presentation and it is very rare to find extra-thoracic lymphadenopathy before the primary tumor, even in advanced cases. Herein, we report a challenging case of a young man presenting with unresolved fever, sore throat, and dysphagia associated with massive pleural effusion, cardiac tamponade, and multiple cervical lymphadenopathy with mesothelial cells ...

 Open Access DOI:10.23937/2378-3656/1410321

Unilateral Blindness: Exceptional Complication of Anti-Vitamin K about a Case

Salmi A

Article Type: Original Article | First Published: September 30, 2020

We report the case of a patient hospitalized for management of orbital hematoma on overdose with oral anticoagulants. With the increase of the hematoma and protrusion of the eyeball, the patient came to ICU, including CT scan of the eye had objectified hemorrhagic infiltration of the orbit, head of exophthalmos. Laboratory tests, found a INR greater than 9. The treatment consisted of a vitamin K antagonist by the associated PFC in default of prothrombin complex concentrate. Ophthalmological, evo...

 Open Access DOI:10.23937/2378-3656/1410320

A Case Arthrogryposis Multiplex Congenita with Renal Affection at Older Age

Abeer Awad Abdellatif, Mervat Essam Behiry and Asmaa Ezzat

Article Type: Case Report | First Published: September 30, 2020

Report on a known case of female patient, 58-years-old, deaf since birth with skeletal deformity presenting with acute kidney injury. These features are consistent with diagnosis of arthrogryposis multiplex congenita. A congenital disease presenting with multiple joint contractures and deformity with deafness and may be renal affection. The second point is that, up to our knowledge, we are the first authors to take into consideration that the arthrogryposis multiplex congenital may be presented ...

 Open Access DOI:10.23937/2643-3907/1710043

Facial Infiltrating Lipomatosis: A Case Report with Natural History of the Disease, Differential Diagnosis and Options for Management

Ashutosh Kumar Singh, Safal Dhungel and Manish Yadav

Article Type: Case Report | First Published: September 17, 2020

Facial infiltrating lipomatosis (FIL) is a rare and underreported clinical entity. Presence since birth and hemifacial swelling and asymmetry is always present along with dentoskeletal hypertrophy. Clinical management varies from conservative liposuction at an early age to aggressive subtotal resection in adulthood. A 21-year-old female patient, operated 3 times before for unilateral facial swelling presented with massive diffuse swelling on the right side of the face. Contrast CT showed infiltr...

 Open Access DOI:10.23937/2377-9004/1410174

In Vitro Fertilization Treatment of a Patient with Primary Partial Empty Sella and Other Co-Factors

Tünde Herman, Péter Török, Antonio Simone Laganà and Attila Jakab

Article Type: Case Report | First Published: September 23, 2020

We report the case of a patient with primary empty sella, who had successful assisted reproductive treatment. The patient is a 28-years-old infertile female with primary amenorrhoea and hypogonadotropic hypogonadism. Serum FSH, LH, E2 indicated central anovulation, but the production of GH, ACTH, TSH and PRL were normal. Obesity and insulin resistance were present. Male partner had asthenozoo-teratospermia and hyperprolactinaemia. After three failed intrauterine inseminations, she was addressed ...

 Open Access DOI:10.23937/2377-9004/1410173

Management of Complete Hydatidiform Mole with Co-existing Fetus

Kaitlin DiBartola, MD, Devin Smith, MD, Kara Rood, MD and David O'Malley, MD

Article Type: Case Report | First Published: September 21, 2020

Complete hydatidiform mole with co-existing fetus (CHMCF) is a rare obstetrical finding. These pregnancies pose a unique set of health concerns including hemorrhage, thyrotoxicosis, preeclampsia, and gestational trophoblastic neoplasia (GTN). In this report, we present a 34-year-old G5P1 presented at 6 weeks and 5 days with vaginal bleeding. Further follow-up revealed a complete hydatidiform mole with co-existing fetus in a patient who desired continuation of pregnancy. There is a lack of data a...

 Open Access DOI:10.23937/2377-9004/1410172

Case Report: Pregnancy While Using an IUD

Elvin Piriyev and Thomas Römer

Article Type: Case Report | First Published: September 19, 2020

Intrauterine contraception, mostly in the form of copper IUD or hormone-releasing system, is a widely used method with a high level of contraceptive security. Despite high contraceptive efficiency, pregnancy can still occur. Pregnancy with a levonorgestrel-releasing intrauterine system (LNGIUS) in situ is very rare. Intracavitary pregnancy with an IUD can lead to a higher risk of infection and preterm birth. We present the case of a 28-year-old woman who was admitted to our hospital due to pregn...

 Open Access DOI:10.23937/2643-4474/1710042

Neuronavigation in Reconstructive Surgery of a Large Skull Defect after Decompressive Craniectomy: Case Report

Zhanna Semenova, MD, PhD and Andrei Marshintsev

Article Type: Case Report | First Published: September 21, 2020

In the absence of autogenous bone due to various reasons, the choice of an implant becomes an important problem of reconstructive surgery. With introduction of computer modelling and development of prototyping technologies the issues of cosmetic reconstructive operations are becoming less relevant. In late cranioplasty implant production and installation is complicated by the presence of significant bone growth along the perimeter of cranial defect. The ability to adjust implant to a bone window...

 Open Access DOI:10.23937/2572-3278.1510044

The Impact of Dairy Elimination on Pediatric Atopic Dermatitis

Aleksandra Nikolovski and Stefan Rallis

Article Type: Case Report | First Published: September 23, 2020

Atopic dermatitis (AD) is a relatively common, inflammatory skin condition of variable severity. Known food allergens such as dairy may play a role in the exacerbation of this T-cell mediated autoimmune condition. A four-year-old patient with severe, non-resolving AD was placed on a dairyfree elimination diet. Quantitative analysis included the use of the Hanifin and Rajka diagnostic tool and the Scoring Atopic Dermatitis Calculator (SCORAD). The patient demonstrated a 76% improvement in her sym...

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