Neonatal lupus erythematosus (NLE) is a rare autoimmune disease due to a passive transfer of maternal autoantibodies to the fetus. Clinical spectrum is variable and includes skin lesions, cardiac, hematological, or hepatobiliary disorders. We report a NLE case presenting with skin eruption that was initially considered as tinea.

We report a unique case of self-healing collodion baby (CB) that was successfully managed despite the risk of potentially serious complications. Self-healing CB is a rare and distinct outcome of collodion phenotype occurring in approximately 10% of the cases. The outcome depends on the initial assessment and adequate multidisciplinary approach.

A 60-year-old woman with bilateral superficial femoral artery occlusion underwent femoral-popliteal bypass surgery. Six months later, left vascular prosthesis occlusion occurred; 1.5 years later, an occlusive embolus developed in the deep femoral artery. The proximal prosthesis aspect was detached from the native vessel. The limb was salvaged with bypass surgery.

We present a rare case of 45-year-old man with complaints of abdominal pain and features suggestive of intestinal obstruction. CT scan of the abdomen demonstrated a large mesenteric mass in the pelvic region involving the distal segment of jejunum. Surgical excision of the lesion and histo-pathological examination confirmed cavernous hemangioma.

Mucoepidermoid Carcinoma (MEC) it can origin from a mandibular odontogenic cyst. We report the case of a 63-year-old man with MEC of the right retromolar trigonum of the mandibula. We performed a wide mandibular excision and immediate reconstruction with a fibula bone free flap.

Primary renal osteosarcoma is exceedingly rare tumor with poor prognosis. It has tendency to spread to distant sites . we report the case of a 43-year-old female who presented with flank pain, gross hematuria, weakness and weight loss and was treated with diagnosis of primary renal osteogenic sarcoma

Metastatic intrathyroid thymic carcinoma (ITTC) is a rare cancer that has no effective drugs. Herein, we report that comprehensive cancer mutation analysis revealed amplification of CD274 gene encoding PD-L1. Multiplex immunohistochemistry also clarified the presence of an immunosuppressive microenvironment via a PD-1/PD-L1 pathway in metastatic ITTC.

Complete agenesis of the permanent canines in the maxilla and the mandible is extremely rare and has only been reported twice. Studies have shown that the incidence of missing canines is more in females. This report describes a sporadic case of congenital absence of maxillary (bilateral) and mandibular (bilateral) canines.

AL represents superficial lymphatic dilatation caused by different processes. It is a consequence of lymphatic damage by an external cause; leading to obstruction of local lymphatic drainage.1 We report a case of AL of the breast in a 45-year-old woman mimicking warts.

It is important to increase the awareness of head and neck surgeons about the recent surge of craniofacial mucormycosis in COVID-19 patients, because early diagnosis and treatment are essential to improve the outcomes. Here, we describe clinical features, treatment protocols, and outcomes of treatment in 8 patients with COVID-19-associated mucormycosis

We report a 24-year-old female patient with a neurological deficit without fever or meningeal syndrome. HIV serology was negative and CD4 count was normal. Cerebrospinal fluid analysis revealed the presence of Cryptococcus neoformans. Neuromeningeal cryptococcosis was suspected. The initial course was favourable with antifungal therapy.

Datura spp. is a potentially poisonous plant that is widely spread and simply accessible, which can yield to poisoning with a central and peripheral anticholinergic effect. We reported cases of family poisoning caused by the herbal tea with refreshing effects that were identified as Datura spp.

Streptococci Group G is an important opportunistic pathogen and causes a wide variety of infections. We discuss a case of recurrent group G streptococcal bacteremia in a 68-year-old male presenting with altered mental status. We also discuss the risk factors, etiology, pathophysiology, diagnosis, and treatment of group G streptococcal bacteremia

Hyoscine butylbromide induced pyschosis, though rare, should be considered in a child presenting with deteriorating cognitive functions and psychotic features acutely as evident in our case of a 9-year-old child taking hyoscine for her non-specific abdominal pain.

Metastatic ovarian cancers could originate from the gastrointestinal tract, and the origin is diagnosed with pathologic and immunohistochemistry evaluation. This case was a woman who was presented with bilateral abdominal masses which were adenocarcinomas originating from GIT. A mass was found in colonoscopy and total colectomy was performed.

Here we present the case of giant multinodular goiter with retrosternal extension in an old lady with dyspnea for 3 months. The patient was treated with Microscopic assisted thyroidectomy without complication.

Peutz-Jeghers syndrome is a rare but potentially life threating syndrome. We report here the case of a young girl who presented recurrent small bowel intussusceptions. Laparotomy exploration showed many jejunal polyps leading to jejunojejunal intussusceptions. These were removed via mini enterotomies and pathological examination concluded to Peutz-Jeghers polyps.

We present the case of a 55-year old male patient who developed hyperkalemia after using Cotrimoxazole(TMP-SMX).He developed an elevated level of potassium from day-4 which kept on increasing until the drug was withheld on day-8.There was a marked increase in levels from 3.0(baseline) to 6.2 before the drug was withheld.