Spinal Cord Infarction During Extracorporeal Membrane Oxygenation：A Case Series and Review of the Literature.

Background: Little is known about extracorporeal membrane oxygenation (ECMO)-related spinal cord infarction (SCI), and reports regarding this rare and catastrophic complication are rare. Here, we report two cases of ECMO-related SCI that occurred between April and December 2023. Data were collected from patients' medical records, with SCI as the endpoint. We reviewed previously published reports by searching PubMed and summarizing the findings. Case summary: One female patient presenting with multiple traumas required oxygenation support through veno-venous ECMO (VV ECMO) due to pulmonary hemorrhage, while one male patient required circulatory support via veno-arterial ECMO (VA ECMO) concurrently with an intra-aortic balloon pump due to cardiac arrest. Neither patient had preexisting neurological deficits; however, upon weaning from ECMO, they presented with severe neurological deficits of uncertain etiology, subsequently confirmed as SCI using magnetic resonance imaging. Conclusion: ECMO-related SCI remains elusive and intricate, and this is the first report of adult VV ECMO-related SCI.

Pneumatosis intestinalis and hepatic portal venous gas in patient with Amanita exitialis poisoning: A case report from Shenzhen, China.

A 57-year-old male admitted as an emergency for mushroom poisoning with hypovolemic shock, acute renal injury (Cr 213 µmol/L) and metabolic acidosis (pH 7.1). Twenty-six hours ago, he consumed 4 caps of wild mushrooms and presented with acute gastroenteritis, generalized malaise and lower limbs jerk. On ICU admission, he developed ventricular defibrillation and was resuscitated with intubation and ventilation. In addition to plasma exchange and hemoperfusion therapy, the patient was managed with massive fluid and potassium replacement, vasopressors, activated charcoal, silymarin, penicillin G and piperacillin tazobactam. On ICU Day 2, the patient's general condition improved with vasopressor ceased, renal function normalized except large amount of diarrhea. On ICU Day 3, the patient deteriorated again with worsening abdominal distension leading to intra-abdominal hypertension (IAH). Toxic liver injury by mushroom became significant. Repeated acute renal injury, deranged clotting and compromised hemodynamics were also noted which indicated acute abdominal compartment syndrome. Emergent computed tomography (CT) of abdomen revealed Pneumatosis intestinalis (PI) in the small intestines and hepatic portal venous gas (HPVG) in the left liver lobe. Water assisted colonoscopy decompression was performed emergently for IAH relief. Thereafter, the patient improved rapidly with organ dysfunction recovered next day. Acute liver failure gradually subsided. On ICU Day 8, the patient was discharged to general ward. The mushroom was later morphologically identified as Amanita exitialis (A. exitialis) by at least two specialists from Chinese Centre for Disease Control and Prevention (CDC). A. exitialis is a lethal mushroom that mainly affect liver and gastrointestinal (GI) tract. The current case and literature review suggest that the severity of GI injury caused by lethal A. exitialis may be underestimated.

An outbreak of Amanita exitialis poisoning.

BACKGROUND: The mushroom Amanita exitialis is reported to cause acute liver injury. It is found in Southern China, and has been previously associated with a high incidence of mortality. METHODS: We described a series of 10 patients with Amanita exitialis poisoning admitted to The Second Affiliated Hospital of the Chinese University of Hong Kong (Shenzhen) in April 2022. Patient demographics, clinical features, laboratory results, therapeutic interventions, and outcome data were collected. RESULTS: Among the 10 patients, 9 survived, while 1 died. Gastrointestinal symptoms were the first to appear (average latency period, 11 ± 4.2 h). Diarrhea was the most common clinical symptom (average duration, 4.4 days). Abdominal distention was an important sign, especially in severely-ill patients. Thrombocytopenia occurred on day 2 after mushroom ingestion and persisted for 3-4 days. Alanine aminotransferase and total bilirubin peaked on days 2-3. CONCLUSION: Amanita exitialis poisoning is characterized by gastrointestinal symptoms and liver injury. In the patient who died, acute hepatic failure led to hepatic encephalopathy and cerebral edema. Abdominal distension accompanied by thrombocytopenia was common in critically ill patients in this outbreak.

A patient with hereditary transthyretin amyloidosis involving multiple cranial nerves due to a rare p.(Phe84Ser) variant.

We report a 30-year-old man involving gastrointestinal symptoms, vitreous opacity, and multiple cranial neuropathies. Transthyretin-related hereditary amyloidosis genetic testing revealed a rare c.251T > C variant p.(Phe84Ser). Only four cases with this variant have been reported before.