COVID-19, TB and HIV are infectious diseases of global public health concern. Triple Co-infection with these diseases can create a diagnostic and therapeutic dilemma. We present a case of a young Cameroonian woman with SARS-CoV-2 -- HIV-TB triple co-infection. Early diagnosis and appropriate management yielded an excellent outcome.

Mesenteric Lipoma is very rare. Diagnosis is challenging because of nonspecific clinical presentation. Complete resection of the lipoma is proposed to relieve pain, and prevent complications. We report a case of mesenteric lipoma revealed by chronic abdominal pain and we performed a litterature review regarding this rare condition.

Gallbladder cancer is a rare but potentially fatal disease. It is often asymptomatic in early stages and is frequently found incidentally or during the workup for benign biliary disease. We present two patients who each had suspicious gallbladder imaging findings and highlight their differences on radiologic and pathologic examination.

Joint involvement in COVID-19 may occur at different stages of the disease and maybe represented by acute arthritis.We report Two cases of COVID-19.Both of our cases are consistent with what has been reported in the literature strengthen the necessity of wider studies to identify rheumatologic manifestations after surviving COVID-19.

Peripheral odontogenic fibroma (POdF) is a rare, benign, and ectomesenchymal tumor. We report a case of a 15-year-old girl who developed POdF in the mandible. The lesion was resected, including the periosteum. Histopathological findings revealed a small mass and cord-like epithelium. No sign of post-operative recurrence appeared after 16 months.

Length of anticoagulation for thrombotic events related to COVID-19 is unknown. We present a patient with COVID-19 complicated by a thrombotic anterior STEMI and multiple left ventricular (LV) thrombi that resolved after 8 weeks of anticoagulation. We suggest a shorter length of anticoagulation with COVID-19 related LV thrombus.

Following surgery for thyroid carcinoma, tracheal necrosis is extremely rare with few reports in literature. We report a patient who underwent a thyroid lobectomy for potential papillary carcinoma, followed by a completion thyroidectomy due to follicular variant papillary carcinoma pathology. Management was successful after debridement and tracheostomy, followed by decannulation.

Charcot foot or neurogenic osteoarthropathy, is a serious complication of diabetic peripheral neuropathy. The association between false aneurysm and Charcot foot is yet uncommon, and has not been reported through the literature. We describe a case of false aneurysm in a Charcot foot in a 55-year-old patient.

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.