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1.
Medical Journal of Tabriz University of Medical Sciences and Health Services. 2018; 40 (1): 97-100
in Persian | IMEMR | ID: emr-205203

ABSTRACT

Plexiform angiomyxoid myofibroblastic tumor is a very rare mesenchymal tumor of stomach which is diagnosed based on morphologic findings such as plexiform growth pattern, spindle cell proliferation in a myxoid background, by aiding immunohistochemistry staining and ruling out of other mesenchymal gastric tumors. We report this tumor with about 4cm size in antrum of a 38 years old man which endoscopic and CT scan results fit with Gastrointestinal stromal tumor and diagnoses is performed according to specific morphologic and immunohistochemistry findings

2.
Medical Journal of Tabriz University of Medical Sciences and Health Services. 2017; 39 (5): 98-102
in Persian | IMEMR | ID: emr-193472

ABSTRACT

Kaposiform hemangioendothelioma [KHE] is an intermediate vascular tumor which occurs in children and commonly associated with Kasabach-Merritt syndrome [KMS]. It commonly occurs in skin, trunk, extremities, and retroperitoneum. We report a 7 months year old boy with a huge intaabdominal KHE without KMS

3.
Tuberculosis and Respiratory Diseases ; : 267-273, 2016.
Article in English | WPRIM | ID: wpr-125742

ABSTRACT

BACKGROUND: Cystic fibrosis (CF) is an autosomal recessive disorder with several clinical presentations. This study was undertaken in the Azeri Turkish population in Iran, to investigate gender differences in the age at onset and diagnosis, age of death, and duration of illness of CF. METHODS: The data of 331 CF patients from 2001 to 2015 was surveyed. Parameters including age, sex, ΔF508 mutation, age at onset, age at diagnosis, age of death and clinical presentations were evaluated for both sexes, using descriptive analysis. The association of gender with these variables was studied using logistic regression, chi-square test and Mann-Whitney U test by SPSS version 18. Odds ratio with a confidence interval of 95% and p≤0.05 was considered statistically significant. RESULTS: The study included 191 males (57.7%) and 140 females (42.3%), all showing statistically significant difference (p<0.001). Age duration differed between genders. Male and female patients were further under 9 and 4 years, respectively. The occurrence of ΔF508 mutation was 0.51 times more in females than in males. Age, diagnosis and sex were closely associated: males were diagnosed at a significantly later age than females (p=0.05). While this compression performed based on clinical presentations, males with respiratory disease had a later median age at diagnosis than females at lifespan (p=0.001). The risk of infertility in males was approximately two times greater than in females (p=0.02). CONCLUSION: These findings indicate gender differences in CF patients. Future studies are needed to establish other differences and evaluate the causes for the gender variations.


Subject(s)
Female , Humans , Male , Age of Onset , Cystic Fibrosis , Diagnosis , Infertility , Iran , Logistic Models , Odds Ratio
4.
International Journal of Women's Health and Reproduction Sciences. 2014; 2 (2): 98-103
in English | IMEMR | ID: emr-148611

ABSTRACT

Primary retroperitoneal mucinous tumors are rare neoplasms and almost exclusively seen in women. In this case report we present two cases of this entity with their clinicopathologic features. The first patient was a 32 years old unmarried woman presented with abdominal pain. Ultrasound imaging demonstrated a solid and thick walled ovarian mass m. 105* 70*80 mm. At laparotomy a large retroperitoneal mass with extention to pelvis, dome of urinary bladder and upper abdomen was found and omentum was involved by the tumor. Histopathological examination revealed a mucinous adenocarcinoma with mural nodule contained high-grade anaplastic carcinoma in retroperitoneal space. The second case was a 36 years old woman with retroperitoneal mucinous cystadenoma. The first case died of disease at first month of her diagnosis. Primary retroperitoneal mucinous tumors that containing anaplastic carcinoma or sarcomas are highly aggressive tumors with poor prognosis showing metastasis by high-grade component


Subject(s)
Humans , Female , Adenocarcinoma, Mucinous/diagnosis , Retroperitoneal Neoplasms , Retroperitoneal Space
5.
International Journal of Women's Health and Reproduction Sciences. 2014; 2 (2): 104-107
in English | IMEMR | ID: emr-148612

ABSTRACT

Echinococcosis is a parasitic disease that is produced by Echinococcus granulosus and still represents an important medical problem in many countries. Echinococcosis in extrahepatic sites is usually asymptomatic unless the cyst causes symptoms due to pressure, as in our case, or ruptures to the peritoneal cavity. Echinococcal cysts at unusual locations many times pose diagnostic dilemmas, and the diagnosis sometimes is made intraoperatively. Primary ovarian and paraovarian cyst hydatid disease is a very rare entity. In our case, a 25-year-old female gravida 1, para 1, was admitted to the emergency department of the Alzahra Hospital of Tabriz due to diffuse abdominal pain, nausea, abdominal distension and urinary frequency of ten-day duration and exacerbation of pain from a few hours before admission. Clinical examination revealed tachycardia of 105 per minute, normal body temperature and normal blood pressure. Abdominopelvic sonography revealed a mass with regular thick contour located in the left ovary suggestive of huge cystadenoma or carcinoma of the ovary. Emergent laparotomy was performed for suspected adnexal torsion. Intra operative findings were a large paraovarian mass with thick wall without any torsion. Mass was removed completely and sent for frozen section study. Pathological examination showed the diagnosis of hydatid cyst. The postoperative period was uneventful and the patient was discharged 3 days later, with the advice to receive Albendazole. The patient referred to a general surgeon for management of the hepatic cysts


Subject(s)
Humans , Female , Ovary , Abdomen, Acute , Laparotomy
6.
Journal of Dentistry-Shiraz University of Medical Sciences. 2014; 15 (3): 112-116
in English | IMEMR | ID: emr-180902

ABSTRACT

Statement of the Problem: Alveolar bone necrosis induced by Herpes zoster infection is considered as a rare manifestation of osteomyelitis and few case reports are presented in the literature


Purpose: The aim of this study was to evaluate mandibular osteomyelitis caused by herpes zoster in the immunocompromised patients with histopathologically documented osteomyelitis in the mandible and herpes zoster infection


Materials and Method: 30 patients were recruited in this cross-sectional study. 19 patients were completely edentulous, 4 patients were partially edentulous and 7 with complete dentition. In all cases, specimens were analyzed using a conventional polymerase chain reaction [PCR] test for varicella zoster virus


Results: 16 patients underwent dialysis, 9 patients received chemotherapy treatments and 5 patients had transplantation [four kidneys and one liver]. Histopathological assessment demonstrated a nonspecific bone necrosis exhibiting an eosinophilic, homogeneous non-vital bone tissue with peripheral resorption surrounded by reactive connective tissue. PCR test was positive in 21 cases


Conclusion: This study demonstrated that the frequency of osteomyelitis induced by herpes zoster could be more than the records provided by previous studies. Histopathological findings might be nonspecific in such patients. PCR test was not positive for all HZ induced osteomyelitis patients

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