Congenital self-healing reticulohistiocytosis of Hashimoto and Pritzker (CSHR), a form of Langerhans Cell Histiocytosis (LCH), is a rare benign proliferative disorder that typically self-resolves at 6 months. We present an atypical case of CSHR with first onset at 10 months of age which showed histologic features of LCH.

Bile leak after cholecystectomy is associated with significant comorbidity. Biliary duct variant anatomy can complicate identification and management. We report a very rare presentation of recurrent delayed bile leaks years after laparoscopic cholecystectomy secondary to missed right posterior sectoral bile duct injury. Surgical intervention was required after failure of conservative management.Key clinical message: Right posterior sectoral duct injury should be considered in patients presenting with a delayed recurrent bile leak. Deep dissection into liver parenchyma during gallbladder fossa dissection should be avoided to prevent occurrence of such injuries.

COVID-19 showed different characteristics and many cases showed clinical manifestations that could not be attributed to other conditions. We present a 22-year-old female had an uneventful recovery from COVID-19 and after that, she developed a cytokine storm and a worsening clinical condition two days after dental root canal therapy.

This report presents a man with a huge coronary fistula, connecting Left Circumflex coronary artery to right ventricle. During the follow-up, the patient developed progressive symptoms of heart failure nonresponsive to medical treatment. Therefore, an endovascular closure with vascular plug was successfully done for him.

Myositis is one of the uncommon adverse events following COVID--19 vaccination, and its mechanism is still unclear. In the hope of aiding in its better understanding, we present a case of myositis following the first dose of the ChAdOx1 nCoV-19 Corona Virus Vaccine, evidenced by serology and MRI.

A 5-month-old German Shepherd dog was presented with cluster seizures. MR imaging showed a large irregular pseudomass in the central region of the cranial cavity, compatible with a malformation of cortical development (MCD). Despite the extensive changes, the patient was neurologically normal interictally one year following diagnosis.

Far migrated IUCD is an uncommon condition that has different manifestations depending upon its location. We present the case of a 22-year-old primipara who had a spontaneous abortion after IUCD placement and suffered chronic right lower abdominal pain thereafter. Diagnostic laparoscopy revealed Cu-IUCD in the right iliac fossa.

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.

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.

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.

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.

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.

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

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.

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.

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

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.

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.