Anapafseos 5 . Agios Nikolaos
Crete.Greece.72100
2841026182
We present a case of gamma-delta T-cell lymphoma that does not fit the current World Health Organization classifications.
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Frostbite may cause lesions. The severity ranges from superficial wounds to severe cases with loss of limbs and tissue. Hence, proper treatment is of utmost importance. We present a case of an 18-year-old man from Arctic Greenland who was admitted with severe frostbite lesions involving both hands. The patient had fallen asleep outside during extreme temperatures. He was treated conservatively with proper wound care, antibiotics and intensive physical therapy. The patient made a full recovery without sequelae. The current report emphasises that non-operative treatment should be attempted for frostbite lesions, as conservative treatment often results in good outcomes.
Haemolytic anaemia caused by a paravalvular leak presenting as progressively worsening red urine. Haemoglobinuria was easily mistaken for gross haematuria, resulting in extensive invasive urological investigation that proved to be futile. Further investigation following an emergency admission led to the realisation that intravascular haemolysis secondary to a paravalvular leakâ"presenting 43 years following metallic valve insertionâ"was the cause of discoloured urine and newly presenting symptomatic anaemia. This case highlights that there remains other causes of what often appears to be haematuria, and further exploration of alternative causes should be considered when no urological cause is found.
A middle-aged man was admitted with worsening hip pain, fevers and reduced mobility. These symptoms were preceded by a mechanical fall but despite regular analgesia, symptoms did not resolve. His prior medical history included ischaemic heart disease, hypertension and hypercholesterolaemia. A trauma and orthopaedic review revealed a painful left hip with reduced range of motion. In addition, some mild tenderness in the left iliac fossa was noted. Blood tests revealed markedly raised inflammatory markers. Plain radiographs and ultrasound were normal. MRI scan found a massive left iliopsoas collection secondary to perforated diverticular disease of the sigmoid colon. The patient was managed with intravenous antibiotics and the collection was drained percutaneously. Approximately 500 mL of pus was aspirated. The patient made an excellent recovery with interval imaging showing a reduction in the collection size.
Thyrotoxic periodic paralysis (TPP) is a well-known complication of hyperthyroidism, characterised by recurrent flaccid paralysis with hypokalaemia. To date, only five cases of this rare disorder have been reported in Saudi Arabia. Here, we report an additional case involving a 25-year-old Saudi man who presented with lower limb paralysis and severe hypokalaemia. Clinically, he showed symptoms and signs suggestive of Graves' disease, which was confirmed by laboratory investigations. Carbimazole, a beta-blocker and potassium replacement were administered, resulting in dramatic improvement of the TTP. This case emphasises the importance of considering TPP in patients with acute muscle weakness and the importance of promptly initiating treatment and preventing relapse of TPP.
Madelung's disease (benign symmetric lipomatosis) is a rare syndrome in which there are multiple lipomas around the neck, upper limbs and trunk in the context of chronic alcoholism. We report on a female patient with lipomas and slightly progressive myoclonus, neuropathy, myopathy, ataxia and respiratory systemic involvement (labelled in the past as Madelung's disease). Multisystem involvement and family history of lipomas led to the development of mitochondrial genetic tests, which can assess two concurrent mitochondrial mutations: the m.8344A>G mutation in MT-TK gene, related MERRF (myoclonic epilepsy with ragged-red fibre) phenotype and m.14484T>C mutation in the MT-ND6 gene responsible for Leber hereditary optic neuropathy phenotype.
Description
Steidele's complex is an eponym to interrupted aortic arch (IAA), which is characterised by complete anatomic discontinuity between the aortic arch and the descending aorta (DA). It is a very rare congenital anomaly that occurs in 19 per million live births.1 Based on the site of interruption, it is classified into three types: type A (30%–40%) when it occurs beyond the left subclavian artery, type B (51%–70%) when it occurs between the left carotid artery and the left subclavian artery and type C (1%–5%) when it occurs between the brachiocephalic artery and the left common carotid artery.2 DA originates from the pulmonary artery through a patent ductus arteriosus (PDA). IAA is invariably associated with a ventricular septal defect (VSD) in majority of cases. IAA is associated with a high mortality rate of 75% at 1 month and 90% at 1 year, in the absence of operative intervention.3 We describe a...
Cystic retrorectal tumours are a very rare entity that pose a problem in differential diagnosis between congenital cyst and other lesions. We present a 49-year-old female patient presenting a perineal bulge which was discovered simulating a vaginal birth associated with prolapsed haemorrhoids grade IV. The interest of this case resides in the surgical indication of a big presacral cyst demonstrated via CT causing acute intense pain due to pelvic organ compression, as no emergent surgery management has been reported up to date.
We present a case of large mass arising from the right pyriform sinus extending inferiorly to the postcricoid area and superiorly to the right aryepiglottic fold causing a foreign body sensation and obstructive symptoms, its histological examination following the endoscopic surgical excision showed a lipoma. We are also describing the endoscopic, radiological and intraoperative findings with a brief literature review.
Acute pneumatosis cystoides intestinalis (PCI) has been described after bone marrow transplantation (BMT). Several case series have demonstrated successful conservative treatment of PCI in children. We present a child with Fanconi anaemia, who developed severe graft versus host disease of the gastrointestinal tract, skin and liver after BMT and an acute, severe form of PCI. Our case report illustrates the complexity of diagnostic and therapeutic procedures in PCI in immunocompromised children.
Description
A 65-year-old man presented with fever and painful swelling at the back for last 2 weeks. His prior history was significant for long-standing type 2 diabetes of 20 years duration and systemic hypertension. Clinical examination showed red, swollen, painful carbuncle with gangrenous patch at the centre and multiple pus points (figure 1). Investigations revealed elevated white blood cell count with neutrophil predominance and high random blood sugar, 340 mg/dL (normal, <140 mg/dL). He was started on insulin and good glycaemic control was achieved. Aggressive debridement of the local affected area was done. Tissue culture was positive for Staphylococcus aureus and he was treated with amoxicillin and clavulanic acid to which he responded well. On follow-up, his debrided wound was granulating well. Carbuncle, also called as infective gangrene of skin and subcutaneous tissue, is most commonly caused by S. aureus that usually starts as a furuncle/boil around the root of a hair...