Bronchial chondromas are very rare pulmonary benign tumors. Despite their rarity, clinicians should pay attention to the possibility of endobronchial tumor in patients with unexplained respiratory symptoms. Treatment modalities for complete excision of the tumor should be initiated to prevent complications and malignant transformation based on the individual tumor situation,

Benign recurrent intrahepatic cholestasis (BRIC) is a rare disease characterized by recurrent severe itching and jaundice. Coronavirus disease 2019 (COVID-19) is a multisystemic acute viral disease and the liver is frequently affected. Here, we wanted to present a BRIC case triggered by COVID-19 infection, discussing it together with current information.

Creatine Kinase (CK/CK-MB) testing is an essential lab test approaching patients with chest or epigastric pain. we report a 38-year-old man with acute pancreatitis and elevated CK/CK-MB level without myocardial involvement. Acute pancreatitis may be considered as a false positive cause of CK/CK-MB test in patients presenting with chest pain.

Patients and their families are discouraged from the restrictions on hospital visits for coronavirus Infection control. This separation might further deteriorate the mental health of both vulnerable patients and their family members. Home care could be a preferable solution to this problem.

Rectal duplication cysts are extremely rare and account for only 4% of all gastrointestinal duplication cysts. They may become difficult for removal in the case of a large tumor in a narrow pelvis. Herein, we report a case of rectal duplication cysts excision via robotic-assisted laparoscopic surgery and its utility.

Title: Multiple nodules in the scrotal wall

Ectopia cordis (EC) is a rare congenital condition characterized by a partial or complete defect of the anterior chest wall. It is associated with ventricular and atrial septal defects (ASD),. This study aimed to explore the cardiac manifestations of EC complicated by coronavirus disease 2019 (COVID-19).

Spontaneous bilateral intracerebral hemorrhage is an outstandingly infrequent context. Ensuing hypertension, trauma inflicted to the brain case is another common cause that out turn into the sequelae of bilateral intracerebral hemorrhage. Lately, a few cases of bilateral basal ganglia bleed have been revealed, as a repercussion of COVID-19 infection.

22 q 11.2 deletion syndrome is a genetic disease associated with a high rate of various psychiatric disorders in addition to multiple physical diseases. This case report suggested that a multidisciplinary team approach is important for perioperative management of patient with 22 q 11.2 deletion syndrome.

An infected tooth that may be deemed unrestorable and may be salvaged by atraumatic removal, an in-hand apicoectomy and retrograde seal, then replantation. Extraction, placing an apical seal and replantation of teeth is not new, nonetheless, clinicians may need to be reminded of this procedure.

Lumbar disc herniation into the dural space is a rare phenomenon of degenerative lumbar disc disease and its pathogenesis remains unclear. Intraoperative ultrasonography and histopathological examination of resected specimen aids in diagnosis of intradural disc herniation.Prompt surgery is recommended as postoperative outcome of the patient at our setting was favourable.

Psychological and psychosocial issues are more prominent issues of an individual in any disease, which could further deteriorate patients’ condition and hamper their quality of life. However, in treating SARS-CoV-2/COVID-19, those patients’ mental, social, and emotional aspects are still overlooked.

Abstract The primary diffuse large B cell lymphoma (DLBCL) of the uterine cervix is extremely rare. In the present study, we described two cases of DLBCL of the uterine cervix in reproductive-aged women complaining of postcoital bleeding, recurrent vaginal discharge, and abnormal uterine bleeding.

Drug reaction with eosinophilia and systemic symptoms (DRESS) is part of Severe cutaneous adverse reactions. Allopurinol, an uric acid-lowering drug, had been incriminated in several cases of Allopurinol-induced Dress syndrome.Through this paper, we present a case of Allopurinol-induced DRESS syndrome with initial oral mucosal involvement.

Periodontal Ehlers-Danlos syndrome type VIII (pEDS) is rare and caused by mutation in complement 1 subunit. Lack of attached gingiva, pretibial plaques, joint mobility, skin fragility, and easy bruising consolidate the diagnosis. We describe a case of de novo-mutation of pEDS with generalized periapical cemento dysplasia (PCD) and leukoencephalopathy.

The clinical and radiographic dilemma of fibrous dysplasia versus osteomyelitis is highlighted in this case of a 4-year-old girl with a bony hard swelling over in mandiblular body and ramus. Differences between histopathological appearance and radiographic presentation with the possible differential diagnosis were discussed and compared with previous studies.

Malignant transformation of mature cystic teratoma (MCTO) is a rare entity. Even rarer is the transformation of MCTO into undifferentiated carcinoma. We report a case of an 80-year-old woman with undifferentiated carcinoma and squamous cell carcinoma component originating from mature cystic teratoma of the ovary.

Combined large cell neuroendocrine carcinoma (LCNEC) and squamous cell carcinoma (SCC) of the H&N is exceptionally rare. We present the case of combined p16 negative SCC and LCNEC of the oropharynx treated with combination chemotherapy. This is the third reported case of combined neuroendocrine carcinoma and SCC of the oropharynx.