Lupus pancreatitis complicated with pseudocyst in a teenage girl, a case report
Keywords:
Lupus Erythematosus Systemyc, Acute Necrotizing, Abdominal PainAbstract
Introduction: systemic lupus erythematosus (LES) is a chronic inflammatory disease of autoimmune nature and unknown etiology, characterized by multiple organ and system involvement and by the presence of antinuclear antibodies. It can appear at any age, with a peak incidence at 12 years of age. The clinical picture of the disease is variable, both in the initial phase and in the course of its evolution. Lupus pancreatitis is one of the rarest manifestations of the disease, its etiopathogenesis is unknown and it is related to vasculitic phenomena, immunocomplex deposition and thromboembolic phenomena.
Objective: to describe the clinical, humoral and imaging evolution of an adolescent girl who presented lupus pancreatitis complicated by the formation of pancreatic pseudocyst.
Case Report: a 17-year-old female adolescent with a personal history of Systemic Lupus Erythematosus Erythematosus since 2021. She was attended at the emergency services of the Pediatric Hospital "Juan Manuel M?rquez", due to abdominal pain in upper hemiabdomen associated with incoercible vomiting and bilious character. She was diagnosed with lupus pancreatitis complicated with pseudocyst.
Conclusions: acute pancreatitis in teenage with Systemic Lupus Erythematosus Erythematosus is a rare complication. Therapeutic actions should be implemented as soon as possible. Although SLE-induced pancreatic involvement is characterized by increased mortality as well as increased disease activity, timely diagnosis of the patient allowed a good outcome. Stomatological surgical risk in patients from office three of the South Area of G?ines, Mayabeque, Cuba
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