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Showing 10 results for Type of Study: case report
Sara Amanpour, Sorena Fardisi, Reza Tabrizi, Mohammad Reza Zarei, Maryam Raoof, Roya Khatami, Volume 2, Issue 3 (8-2015)
Abstract
A rare case of squamous cell carcinoma ex pleomorphic adenoma in maxillary sinus is presented. The patient is a 50-year-old woman presenting with a slow-progressive swelling in left side of her face that she has noticed 2 years earlier. The lesion was not painful and caused asymmetry and mild exophthalmos. Microscopic examination revealed that the tumor was composed of two components partly of a pleomorphic adenoma and partly of a squamous cell carcinoma. Immunohistochemical examination for Ki-67 and SMA and mucicarmin staining were also done and confirmed the diagnosis of carcinoma ex pleomorphic adenoma. There is no evidence of recurrence 12 months after operation.
Kourosh Sayehmiri, Mohammad Reza Kaffashian, Elahe Ranaei, Volume 3, Issue 2 (3-2016)
Abstract
Introduction: Congenital anomalies are a common cause of disability and mortality in newborns and their treatments involves high costs for the society. This study aimed to investigate the prevalence of congenital anomalies and their causes.
Materials and methods: This research was a descriptive-analytical study and the population included all the newborns in hospitals of the city of Ilam in 2011. Variables of abnormality type, birth status, and medical and genetic illness histories were included into the data collection forms. Data was analyzed through Chi-square tests and Fisher's exact test using SPSS software.
Results: Of 460 neonates, 5.4 percent (25 cases) had died at birth and 3.7 percent (16 infants) were born with a birth defect. 43.8 percent of malformed babies had a family history. 31.3 % of the malformed babies had genetic syndromes, whose parents had consanguineous marriage. 18.8% of babies with defects in the central nervous system and cardiovascular system showed a similar percentage of disorder. The defect in the urinary system, head and neck each accounted for 12.5 percent.
Conclusion: This study shows that consanguineous marriages can be the most common genetic cause of genetic syndromes.
Mahmood Akhlaghi, Volume 3, Issue 4 (9-2016)
Abstract
Anisocoria during anesthesia is very rare, but may indicate life-threatening neurologic injuries and create tremendous condition. A 23-year-old male patient was anesthetized with fentanyl and propofol. Thirty minutes after inducing anesthesia, unilateral mydriasis was detected. The duration of surgery was shortened for prompt evaluation of the pupils. At the end of the operation neither vision problem nor obvious anisocoria was detected in the recovery room. Ophthalmological and neurological consultations revealed no pathological finding and the patient was discharged. Evaluation of the size of the patient's pupils before operation would mitigate the fearful condition resulted from anisocoria.
Elham Naghshineh, Mehrdad Mostaghaci, Volume 4, Issue 2 (3-2017)
Abstract
A 28 years’ pregnant woman with 24 weeks’ gestational age referred with petechiae and purpura from previous day without any trauma. She had an occipital headache from last night. Overt petechial and purpuric lesions were seen in the mouth and skin. There was neither hepatosplenomegaly nor lymphadenopathy. She was conscious and oriented. The patient was febrile, anemic and thrombocytopenic with stable vital signs. All liver enzymes were elevated. Coagulation profile was normal. WBCs were normal. RBCs were reduced, and she had polychromatosis. Overt shistocytosis was seen. Platelets were significantly decreased. The first diagnosis was TTP. All necessary laboratory tests were done to rule out the secondary rheumatologic causes of TTP; which all were normal. Coombs tests were negative. ADAMTS 13 Ab was elevated. Fetal ultrasonography was normal.
Treatment started with plasmapheresis and corticosteroid. After treatment, platelets count begins elevated, and LDH decreased. The patient discharged with a good general condition and normal lab tests. She continued her pregnancy until term, and born a normal infant without any complication. She did not have a recurrence of TTP until September 2014.
Behnaz Nateghi, Reyhaneh Rabieian, Mansoor Salehi, Volume 6, Issue 4 (9-2019)
Abstract
Chronic lymphocytic leukemia (CLL) is the most common leukemia in adults. Anemia is world health problems and common medical conditions seen in clinical practice. We report the case of a 47-years-old woman who presented pain and obvious changes in hallux. With regard to available symptoms, special issues like strike, CLL, banned veins of foot and occult blood was guessed as a general mechanism of disease. But the result of performed tests and the effect of used drugs exclude all mentioned problems and low hemoglobin level was recognized as the only crucial cause of disease. With according to the results of blood counts and symptoms, disease for CLL, after performing tests and treatment of disease with iron supplementation, we recognized that particularly iron deficiency is the essential cause of disease.
Zeinab Mohammadzadeh, Elham Maserat, Volume 7, Issue 2 (3-2020)
Abstract
Dear Editor,
Shortly after the first outbreak in China, the Corona virus has affected many countries around the world. The first confirmed case of the virus in Iran was reported in Qom on February 2020, and then it spread to other cities in Iran. The outbreak has caused many social and economic challenges for the international community; also, there is no complete information about this disease.
One of the most important challenges is the prevalence of inaccurate information about the disease, which has many psychological, political, social and economic effects on society. Infodemic or the spread of wrong information about the disease through various social media in the global community is a serious problem for public health.
The dissemination of information can severely affect people's behavior and alter the effectiveness of governments’ countermeasures. In this present letter was reviewed integrated portal as a one of the solutions to infodemic management. The use of authentic sources to provide accurate information in the community is one of the best approaches to combat this phenomenon. Timely information sharing and comparison of epidemiological and genomic data on infectious diseases leads to faster and more efficient control of global outbreaks and disease tracking. In spite of all the problems in this area, various solutions have been proposed for this issue.
The portal is one of the significant technologies which provide correct and required data for different users. Web portals are increasingly becoming part of modern life. Portals collect uniform information from multiple sources and provide consistent access to multiple information, software and applications from different databases to organizations and community. Portal content is available from a variety of tools such as PCs and smartphones. For example, government web-portals can be used by public and private organizations. Many studies have confirmed the usefulness of portals for managing infectious and chronic diseases, if it is designed according users need.
The accurate and comprehensive information sharing with all stakeholders and health organizations such as WHO about Covid-19 is essential for better management of the disease.
One of the applications of portals is sharing of accurate and reliable information by responsible authorities for managing this disease. Justice must be respected in presenting results of recent research on Covid 19, and everyone has equal access to this information according to their role in society. By sharing the results of scientific research, the general public are also preparing themselves to fight the disease.
In recent days, various applications, soft wares and websites have been provided by the relevant organizations for the effective management of CVD 19. The integration of these technologies into comprehensive portal is essential for a comprehensive management of disease.
The portal will be accessible to public, patients, providers and policy makers. It can prepare educational, medical, and research information for users.
Some benefits of portal including information gathering from various sources, availability of information for all user groups (general and specific users), uploading information by users according to the access level, designing customized pages by users or groups, decreasing the attendance of patients and public in high risk areas, increasing information security, reducing people's confusion about finding the required information and facilitating communication.
Alireza Ghodsi, Bita Dadpour, Zahra Shokri Toroghi, Volume 7, Issue 3 (6-2020)
Abstract
Aluminum phosphide (ALP) is a very toxic compound commercially accessible as "rice tablet" in some markets in Iran. Although this toxin is used as a pesticide to protect grains from pests, it may be used for committing suicide. The poisoned patient experiences gastrointestinal problems as the first clinical manifestations in case of oral use, then develops acid-base disturbance, shock, and death in many cases. Intoxication with ALP can also affect the patient's hemodynamic status and cause electrocardiograph alterations, dysrhythmias, and even myocardial necrosis. In the current study, we introduce a young man who consumed an ALP tablet in a suicidal attempt and developed myocardial infarction even before metabolic acidosis and hypotension.
Mahtab Sadeghipour, Reihaneh Barani Toroghi, Zohreh Sadeghipour, Mehdi Rostami, Akbar Azizifar, Volume 10, Issue 2 (3-2023)
Abstract
Introduction: Mental disorders in people who stutter are controversial among researchers. The 3 types of stuttering are developmental stuttering, neurogenic stuttering, and psychogenic stuttering. The exact cause of stuttering is unknown. This study aimed at investigating the relationship between Stress and Reading Comprehension Performance of Iranian Stuttering Individuals.
Materials and Methods: The current research was descriptive quantitative research with a correlational approach. The research tools included Zong's Self-Rating Anxiety Scale (S.A.S) questionnaire. The face validity, reliability and internal consistency of the questionnaire were examined. Five patients (5 adult men aged 14 and 19 with symptoms of stuttering and stress) were selected voluntarily among those who referred to the speech therapy clinic in Ilam.
Results: To test the normality and abnormality of the research data, the Kolmogorov Smirnov statistics for stuttering and stress were 0.176 and 0.198, respectively, and the significance levels for both variables were greater than 0.05, none of which were statistically significant. In other words, the normality of the data was confirmed, which showed that Pearson's parametric tests can be used. The results indicated a relationship between stress and vulnerability (P < 0.05).
Conclusion: It has been concluding that there is a significant relation between stress and stuttering, indicating that stress and social phobia are common among people who stutter.
Azita Mazaheri Tehrani , Arash Zarbakhsh, Verishe Rastin, Hamed Karimi, Volume 10, Issue 4 (12-2023)
Abstract
Introduction: Body defects impact well-being, necessitating efficient prosthetic techniques. This report explores integrating CAD/CAM technology for auricular prostheses, emphasizing a digital approach.
MaterialS & Methods: The plan involved irreversible hydrocolloid impressions, generating a digital resin model through an indirect scanner. Traditional molding and 3D printing combined for pattern formation. The mold's investment, fabrication, and coloring used intrinsic and extrinsic painting.
Results: CAD/CAM showcased enhanced compatibility and aesthetics. The digital resin model improved adaptability, streamlining production, and accelerating the wax try-in process. Patient satisfaction during follow-ups validated the prosthesis success.
Conclusion: Exploring auricular prosthesis advancements via digital technology, particularly the digital resin model, demonstrated transformative outcomes. This approach not only enhances adaptability and aesthetics but also expedites production, promising a seamless and time-efficient restoration of ear aesthetics for individuals.
Amir Hossein Kasaian Naini , Sina Salat, Parastoo Tajzadeh, Siavash Nickfarjam, Golnaz Khodadadian, Mohsen Arefnezhad, Volume 12, Issue 1 (1-2025)
Abstract
Background: Hydatidosis is a parasitic disease caused by the larvae of the genus Echinococcus. Hydatidosis commonly affect the liver and lungs, but can occur in any part of the body, including rare sites like musculoskeletal tissue.
Case Report: We reported a case of a 42-year-old male nurse with a painless mass in the anterior region of his right thigh that developed between 2009 and 2023. No history of trauma, lesions, walking difficulties, or impact on daily activities were observed. He lives in Bandar Abbas, Southern Iran, and was admitted to Abolfazl Hospital in Kashmar. The preoperative diagnosis was lipoma. Blood tests were normal. Both sonography and magnetic resonance imaging detected multiple cysts measuring (140*45 mm) and (144*51*32 mm), respectively. Imaging exams showed the size, shape, and location of the cyst. Hydatid cyst was diagnosed after surgery. Histopathological examination confirmed a Hydatid cyst diagnosis.
Conclusion: Hydatid cysts in muscles could occur rarely in muscle (0.5-2.5%). Thus, it's important to consider Hydatidosis in the differential diagnosis of soft tissue masses in low-prevalence areas.
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