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Abstract Number: C33
THE COPYCAT DISEASE: A CASE OF LUPUS PODOCYTOPATHY
SHM Converge 2022
Case Presentation: Lupus nephritis (LN) is a clinical manifestation of SLE that can be histologically categorized from class I-VI. One form of LN that is not included in the classification is lupus podocytopathy (LP). LP is a somewhat rare manifestation of SLE associated nephrotic syndrome that mimics minimal change disease (MCD) and is diagnosed via [...]
Abstract Number: H36
MILWAUKEE SHOULDER SYNDROME IN 41 YEAR-OLD WITH END STAGE RENAL DISEASE
SHM Converge 2022
Case Presentation: A 41 year-old female with a history significant for end stage renal disease (ESRD) secondary to focal segmental glomerulosclerosis (FSGS) on peritoneal dialysis for two years, uremic pericardial effusion with pericardiocentesis three years prior, and polyarticular gout on allopurinol presented as a transfer from an outside hospital for evaluation due to concerns for [...]
Abstract Number: M31
A CASE OF ANTI-MELANOMA DIFFERENTIATION ASSOCIATED GENE 5 DERMATOMYOSITIS
SHM Converge 2022
Case Presentation: Anti-melanoma differentiation-associated gene 5 dermatomyositis (MDA5-DM) is a subset of amyopathic dermatomyositis that may present with oral ulcerations, painful palmar papules, arthritis, and panniculitis.1 Unique characteristics of MDA5-DM versus other types of dermatomyositis include a higher incidence of interstitial lung disease (ILD), lower incidence of myositis, and a higher rate of morality. MDA5-DM [...]
Abstract Number: P42
MISSED DIAGNOSIS OF SYSTEMIC SARCOIDOSIS CAUSING SEVERE PANCYTOPENIA AND MACROPHAGE ACTIVATION SYNDROME DURING PROLONGED HOSPITALIZATION
SHM Converge 2022
Case Presentation: A 59 year old woman with presumed systemic lupus erythematosus (SLE) was admitted to hospital medicine for severe pancytopenia (WBC 1.3 x109/L, hemoglobin 9.2g/dL, platelet 14×109/L). She had an extensive diagnostic work-up with rheumatology and hematology without a definitive diagnosis; rheumatology questioned her prior SLE diagnosis. Imaging showed diffuse lymphadenopathy and splenomegaly. Three [...]
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