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235 Possible Causes for Erythematous Rash, Metabolic Acidosis

  • Acute Kidney Failure

    Medical treatment for hyperkalaemia and metabolic acidosis was initiated as well as plasma volume expansion.[] […] symptoms should be looked for in diseases such as Systemic Lupus Erythematous (SLE) and the vasculitides.[] Although correction of an anion gap metabolic acidosis with sodium bicarbonate is controversial, correction of the nonanion gap portion of severe metabolic acidosis (pH 7.20[]

  • Multiple Carboxylase Deficiency

    A 30-month-old female patient who presented with the initial features of diabetic ketoacidosis (severe metabolic acidosis, ketosis, and hyperglycemia), lactic acidemia, moderate[] rash with skin exfoliation and alopecia, failure to thrive, seizure, coma, developmental delay, foul smelling urine, metabolic acidosis, ketosis and hyperammonemia.[] If not, it can result in irreversible damage to the central nervous system and early death from metabolic acidosis.[]

  • Short Bowel Syndrome

    Persistent metabolic acidosis and mineral and bone disorders should be of particular concern in hemodialyzed patients with SBS.[] Also, a scaly erythematous rash can erupt around the mouth, eyes, nose, and perineum. Weser E. Nutritional aspects of malabsorption: short gut adaptation.[] Zinc deficiency - angular stomatitis, poor wound healing, alopecia, scaly erythematous rash around the mouth, eye, nose and perineum.[]

  • VIPoma

    Laboratory tests revealed high vasoactive intestinal peptide (VIP) hormone levels, hypokalemia, and metabolic acidosis.[] Necrolytic migratory erythema is an erythematous rash, which typically begins in the groins and perineum and migrates to distal extremities, forming bullae which heal with[] Laboratory investigations revealed high VIP hormone level (989pg/mL), hypokalemia, hypercalcemia, hyperglycemia, high blood urea nitrogen, high creatinine, and metabolic acidosis[]

  • Diabetic Ketoacidosis

    Metabolic acidosis in an infant requires a broad differential. Rasburicase should be considered in hyperuricemia and DKA.[] We describe a previously healthy adolescent boy who presented with respiratory distress, hypotensive shock, and a diffuse erythematous rash.[] Both patients had normalization of their ECGs after treatment of marked electrolyte abnormalities and metabolic acidosis.[]

  • Hepatitis B

    On admission, a complexity of multiple fractures, hypophosphataemia, glycosuria without hyperglycaemia and non-anion-gap metabolic acidosis indicated a diagnosis of acquired[]

  • Allergic Interstitial Nephritis

    Other conditions that may develop include a high concentration of potassium in the blood, metabolic acidosis, and kidney failure.[] . • Erythematous maculopapular skin rash, fever, arthralgias, peripheral eosinophilia(Drug induced). • Microscopic haematuria and pus cells. • Eosinophils 1% of the cells-[] acidosis, progression to ESRD.[]

  • Pyruvate Carboxylase Deficiency

    Pyruvate carboxylase deficiency, complex form, presents in early infancy with lethal metabolic acidosis, resulting from ketoacidosis and lactic acidemia.[] The juvenile form presents with lactic acidosis, alopecia, intermittent ataxia; seizures; and an erythematous rash.[] The patient developed signs of severe liver damage and died at 13 days of age after increasing metabolic acidosis and severe bleedings.[]

  • Pseudohypoaldosteronism of Infancy

    PHA presents hyponatremia, hyperkalemia, and metabolic acidosis, accompanying with high urinary sodium, low potassium excretion, and high plasma aldosterone concentration.[] Fig.1 Erythematous papular rash resembling Miliaria rubra on the abdomen and arms of the baby.[] Laboratory features include: Hyperchloraemic metabolic acidosis. Metabolic alkalosis with or without hypokalaemia. Hyponatraemia with hyperkalaemia.[]

  • Hyperuricemia

    Metabolic acidosis in an infant requires a broad differential. Rasburicase should be considered in hyperuricemia and DKA.[] rash, fever, hepatitis, eosinophilia, or acute renal failure.[] We report on a 16-day-old male with metabolic acidosis, hyperuricemia, hyperuricosuria, and nephrocalcinosis caused by Lesch-Nyhan syndrome.[]

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