Our patient is a 39-year-old male with normal baseline blood parameters who presented with COVID-19 infection, associated with neutropenia and then progressed to critical disease culminating into CSS. Based on risks and benefits evaluation, he was treated with Tocilizumab reinforced with G-CSF leading to full recovery including reversal of neutropenia.

We report a case of a 41-year-old male patient with no family history, presented with extensive multiple keratoacanthomas with disfiguring scars. The diagnosis of a sporadic form of Ferguson-Smith syndrome was made. Treatment with acitretin showed a marked response. Recognizing this syndrome is crucial, early treatment helps avoid scar format

Serum prostate-specific antigen (PSA) plays an important role in the screening and diagnosis of prostate cancer (PCa). The recommended PSA cut-off in PCa screening is 4ng/ml. We report two cases of low PSA localized PCa which were incidentally found by computed tomography (CT) taken for another disease.

In receptors of solid organ transplant, calcineurin inhibitors has become a pillar of immunosuppressive treatment. Several case reports have shown hypertrophic and dilated cardiomyopathy as a side effect of tacrolimus. We present the case of a woman receptor of a kidney transplant who developed hypertrophic cardiomyopathy due to Tacrolimus.

Omphalolith is a rare and underdiagnosed entity due to the accumulation of sebum and keratin in the umbilicus. It usually occurs in the elderly with deep and narrow umbilicus. Early recognition of omphalolith is important to prevent complications, unnecessary investigations and anxiety. We report herein two new cases of omphalolith.

We report the case of a 65-year-old woman who presented to our hospital with a complaint of abdominal pain due to undigested mochi, which was resolved by snare cutting.

Stevens–Johnson syndrome (SJS) with respiratory distress can lead to fatal outcomes. However, there are a few reports of drug-induced lung injury with diffuse alveolar damage caused by acetaminophen, the most severe type. Here, we describe a fatal case of acetaminophen-induced SJS in a child with irreversible lung lesions.

Anti-glutamic acid decarboxylase(Anti-GAD) are associated with various neurologic condition; but, no meningitis has been reported with it, so far. Evidence demonstrates the associated of autoimmune meningoencephalitis with Covid-19 infection. Here we report a 44-year-old female with progressive loss of consciousness with anti-GAD65 meningoencephalitis after Covid-19 infection.

Yersinia pseudotuberculosis is a rare Gram-negative bacillus that cause enterocolitis and terminal ileitis. We report the first Danish case with Y. pseudotuberculosis multiple pyogenic liver abscess presenting with six weeks intermittently fever, fatigue and weight loss. The patient was successfully treated with percutaneous drainage and intravenous piperacillin/tazobactam and oral ciprofloxacin.

In the laryngeal foreign body caused by plate-shaped grilled liver, computed tomography imaging showed the presence of air along the pharyngeal wall between the wall and the meat, which can be mistaken as pharyngeal emphysema.

Marfan syndrome (MFS) an inherited disorder caused by FBN1 gene mutations, is well known to cause lethal aortic aneurysm and dissections at a relatively young age. Here, we report giant internal carotid artery aneurysms and porcelain aorta in an elderly patient with MFS.

Erythema multiforme is a reactive inflammatory mucocutaneous disorder. It is etiology varied from bacterial, viral or fungal infection to drug reaction. The aim was to report a case of drug induced oral erythema multiforme, in order to highlight it's clinical and histological features in addition to the therapeutic modalities.

Solitary fibrous tumours (SFT) are a rare group of spindle cell neoplasm of submesothelial origin with malignant potential. Here, we are presenting a case of a 45-years-old male patient, who presented with recurrent episodes of hypoglycemia spells and later on, it was diagnosed that hypoglycemic spells were secondary to fibroma.

DERMATOFIBROSARCOMAPROTUBERANS (DFSP) is a rare recurrent fibrohistiocytic tumor. Given the limitation of available diagnostic modalities in a resource poor setting, diagnosis can be confusing. As most of the tumors recur with time, our case of complete cure was interesting phenomenon observed in our case

This case report displays some of the possible complications of sumatriptan poisoning, including nephritic syndrome.

A 65-year-old male with history of Hashimoto's thyroiditis on Levothyroxine developed Graves' disease with ocular symptoms and was treated with teprotumumab without improvement. Total thyroidectomy was performed to control hyperthyroidism. Surgical pathology revealed multifocal papillary thyroid carcinoma. Rarely a spectrum of thyroid disorders is seen in a single patient.

Our study of a patient who experienced a torpid evolution in 9 months incomplete treatment with antimonials and amphotericin B, with the destruction of the eyeball, a large area of necrosis on the face and nasal bone exposure.

We report  8-year follow-up of a home-based exercise rehabilitation program combined traditional Chinese medicine for a patient with triple vessel disease patient complicated with heart failure without invasive intervention. Improvements were observed in all outcomes.