Articles

Volume-5, 2024
Issue 1 (January)



Sinusoidal obstruction syndrome of the liver successfully managed by defibrotide during chemotherapy in a child with Hodgkin lymphoma with liver involvement: A case report and review of the literature

Sinusoidal Obstruction Syndrome (SOS) of the liver is a life-threatening disorder generally occurring as a complication of Hematopoietic Stem Cell Transplantation (HSCT). Here, we describe a case of a child with Hodgkin’s lymphoma and liver involvement who developed SOS during induction chemotherapy outside the transplant context, which is a very unusual presentation in pediatric patients.

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Unidigital severe lichen planus vulgaris: “Tincture of timing”

Lichen Planus is a multifaceted mucocutaneous auto immune inflammatory disease of multiplex etiopathogenesis. Nail involvement is seen in up to 10-15% of patients. Most cases are mild, and serious consequences may occur due to swift progression of the disease, the high risk of scarring, and resulting in permanent damage to the nail architecture (4-12%).

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Pulmonary actinomycosis masquerading as lung cancer

Pulmonary actinomycosis is a rare chronic purulent granulomatous disease, which can be easily misdiagnosed as lung cancer, tuberculosis, and other diseases. However, diagnosis relies on histopathological evidence, and early diagnosis is conducive to the patient’s recovery.

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Klebsiella aerogenes is indeed a gas producing bacteria

Pancreas cancer with peritoneal involvement was found in a 64-year-old man for which he received 5-fluorouracile, folinic acid and oxaliplatin. One month later, the patient was referred to ICU for shock. Examination revealed intense abdominal and right scrotal pain. The patient received fluids, norepinephrine and intravenous piperacillin-tazobactam.

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Hirschsprung disease with recurrent obscure gastrointestinal bleeding

Hirschsprung Disease (HD) is a form of colonic aganglionosis with an incidence of 1 in 5000 liver births. It presents as constipation since birth with other intestinal and extraintestinal disorders. Here we present a case of a 22-year-old female who presented with constipation since birth and repeated episodes of melena requiring a total of eight units of blood transfusion for the last six years. There was a history of prolonged defecation and digital evacuation of stool.

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A rare case of multiple myeloma of vertebral bodies with cervical canal stenosis

A 70-year-old male patient presented with bilateral lower limb weakness that progressively extended to the upper limbs. This weakness was accompanied by an inability to walk or stand, back pain, followed by paraparesis and paraplegia. He also experienced urine retention and no passage of stools or flatus, along with an episode of fever and weight loss.

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Clinico-pathological characteristics of triple negative breast cancer: A retrospective study of 50 cases

Retrospective study aimed to investigate the anatomoclinical features of triple negative breast carcinoma and compare them with data in the literature. An exhaustive retrospective study of 50 cases of triple-negative breast cancer diagnosed in the Pathology Department at the Mohammed V Military Training Hospital in RABAT, for five years and 08 months from January 2018 to August 2023.

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Infantile scapulothoracic dissociation

Scapulothoracic dissociation is rare but a limb-threating injury that usually occurs after high energy trauma. Our case was 2 year olds after low energy trauma with axillary mas and restricted movement of the right shoulder and radiographic finding showed that the scapula was displaced laterally.

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Pitfalls in FDG-PET/CT: Unique brown fat activation due to a β3-adrenergic receptor agonist in a patient with treated uterine cervical cancer

Brown Adipose Tissue (BAT) activation with increased uptake on FDG-PET/CT studies is a well-known phenomenon. Activated BAT is usually seen in the supraclavicular region, but also in Para spinal and mediastinal locations, and rarely in perirenal sites. Here, we report a unique case of atypically intense, multilocular FDG uptake in activated BAT

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Systemic artery to pulmonary artery fistula

A 33-year-old female presented with four years of shortness of breath. She denied sputum production, fever, chills, chest pain or hemoptysis. She was diagnosed with pulmonary embolism four years prior, treated with anticoagulation for six months. Physical examination was remarkable for sinus tachycardia.

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Chilaiditi syndrome: A simple chest x-ray image makes the diagnosis

Chilaiditi syndrome is the colonic interposition to the liver reaching the under-surface of diaphragm with associated abdominal pain; it is one of the causes of pseudopneumoperitone- um. This clinical manifestation distinguishes chilaiditi syndrome from asymptomatic colonic interposition, which is termed as chilaiditi sign [1,2].

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A simultaneous bilateral total knee replacement: The road to recovery

The patient had suffered from arthritis in both knees for several years. In discussions between the patient and the orthopaedic surgeon the decision was made to carry out a simultaneous bilateral complete knee replacement. Epidural anaesthesia was employed to remove feeling from the lower part of the body. The operation was completed successfully.

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A case report of delayed-onset delirium tremens

In a 68-year-old male patient with long-term drinking, he appeared tongue tremor, hands shaking, hallucination, clarity of consciousness decline, disorientation at 12 days after stopping drinking, after discussion in our ward, his diagnosis was identified for delirium tremens. He was given the treatment by diazepam, high doses of B vitamins.

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Re-expansion pulmonary oedema: A rare complication

A 48-year-old female patient, with a medical history encompassing familial amyloidotic polyneuropathy and heart failure, became the focal point of a complex medical narrative. Admitted due to a symptomatic increase in right pleural effusion, accompanied by contralateral deviation of the mediastinum.

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Arthroscopic resection of large synovial hemangioma in the posterior recess of the left knee via median and double posteromedial portals: A case report

Synovial hemangioma is a rare benign tumor. This case report describes a 27-year-old woman who was admitted to the hospital with a 1-year history of pain in the popliteal fossa of the left knee and mobility limitation. According to the medical history and MRI examination, the patient was diagnosed as synovial hemangioma of the left knee.

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Osteonecrosis of the lunate bone

Osteonecrosis of the lunate bone or lunatomalacia, it is also known as Kienbok disease. The mechanisms by which this disorder develops are not fully understood, compromise of the bone vasculature is the most commonly proposed cause.

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Striae rubrae due to cushing’s syndrome

A 29-year-old man was referred by his primary care physician for hypertension resistant to antihypertensive drugs. For 1 year he had been suffering from bradypsychia, dizziness, asthenia, adynamia, muscle weakness and weight gain.

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Gallstone ileus due to duodenal diverticulosis

A gallstone may form within a duodenal diverticulum, entering the bowel without the presence of a biliary enteral fistula. This can result in a small bowel obstruction known as “gallstone ileus” but characterized by a normal gallbladder and no pneumobilia.

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The potential protective role of lactate in the early onset of intensive care unit-acquired weakness (ICU-AW) in patients with shock

The objective was to investigate the correlation between early lactate levels and the early development of Intensive Care Unit-Acquired Weakness (ICU-AW) in patients with septic shock. Data from pneumonia-induced septic shock patients in our ICU were analyzed, dividing them into ICU-AW and non-ICU-AW groups based on ICU-AW development within 7 days.

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Superior mesenteric artery syndrome: A case report

Superior Mesenteric Artery (SMA) syndrome, also known as Wilkie’s syndrome, is a rare condition of duodenal obstruction due to extrinsic compression of the third portion of the duodenum by the superior mesenteric artery and the abdominal aorta.

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Cisco brazier-induced Erythema Ab Igne

Erythema Ab Igne (EAI) is a skin condition manifested by net-like darkening due to continuous exposure to moderate temperatures generated by various heat sources which predominantly appear in the calf area and distal region of the lower extremities. EAI diagnosis is clinical and treatment consists of removal of the heat source.

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An unusual course of rituximab

Rituximab (RTX) is increasingly used to manage autoimmune diseases and haematological malignancies [1,2]. Contrary to the common adverse effect of hypersensitivity reactions and infection, late-onset complications of rituximab are rarely reported.

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Mees’ lines transverse leukonychia

A 56-year-old man was admitted to the hospital for acute decompensated heart failure and acute kidney injury. He had a history of smoking, hypertension, and obesity. He was diagnosed with acute myocardial infarction and received medical treatment.

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The great mimicker: Acute catatonia secondary to acute hypoglycemia

A 58-year-old man with diabetes and human immunodeficiency virus presented to the emergency department in a state of acute catatonic rigidity, with the inability to speak, and the inability to relax his upper and lower limbs with gravity. Bedside glucometry revealed a blood sugar level of 29 milligrams per deciliter.

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Neonatal suppurative parotitis: Case report and review of literature

Neonatal suppurative parotitis is a rare entity, its diagnosis is essentially clinical with a good prognosis usually. We report a case of a 21-day-old female whose been taken care of in our department for neonatal suppurative parotitis presenting with feverish, hard, red, tender swelling of the parotid loge.

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Flail chest in posterior segment

A 35-year-old male reported to the emergency department after a road traffic accident with complaints of chest pain on the left side and breathing difficulty. On the primary survey, his GCS was full, his airway was patent, breathing spontaneously with a respiratory rate of 28/min with paradoxical movement.

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A case of a large and kidney-shaped thoracic mass

A 60-year-old woman with a high-grade myxofibrosarcoma of her left forearm, submitted to surgical excision and postoperative radiotherapy, presented to the emergency department, after 3 years, with a 2-months history of progressive asthenia and shortness of breath.

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