Pre-season Flashcards
ANA pattern of SLE
Peripheral (rim) pattern
Remark/s on SLE manifestations
Oral or nasal ulcers: usually painelss
Joint disease: nonerosive synovitis involving 2 or more peripheral joints
Renal disorder: persistent proteinuria >0.5 g/24 hours, or red cell casts
WBC <4000 on 2 or more occasions
Plt <100
Class I lupus nephritis
Minimal mesangial
Class II lupus nephritis
Mesangial proliferative
Class III lupus nephritis
FOCAL
<50% of glomeruli
Subendothelial IC deposits
📌similar with †MPGN I (subendothelial deposits)
†double contour, tram-track GBM on LM
Class IV lupus nephritis
DIFFUSE
>= 50% of glomeruli
Subendothelial IC deposits
Similar with †MPGN I’s subendothelial deposits
†double contour, tram-track GBM on LM
Class V lupus nephritis
MEMBRANOUS
LM: Diffuse capillary thickening
IF: subepithelial IC deposits 📌
PSGN: subepithelial HUMPS
*Membranous nephropathy:
Subepithelial deposits (spike and dome appearance)
- 2nd most common in adults
- assoc’d with SLE, infections (HBV, HCV, T pallidum, schistosoma, plasmodium)
Class VI lupus nephritis
ADVANCE SCLEROSING
Sclerosis of >90% of glomeruli
Antibodies in diffuse cutaneous systemic sclerosis
Anti-DNA topoisomerase I
Anti-Scl 70
Autoantibody in limited cutaneous systemic sclerosis
Anti-centromere antibodies
“Limited scleroderma
Acute antibody-mediatied transplant rejection
Inflammation of glomeruli and peritubular capillaries with focal thrombosis of small vessles
Remark/s on digeorge syndrome
CATCH 22 Cardiac defects Abnormal facial features Thymic hypoplasia Cleft palate Hypocalcemia Deletion in chromosome 22q11.2
Remark/s on Wiskott aldrich syndrome
TIE the WASP
Thrombocytopenia
Infections, recurrent
Eczematous dermatitis
Desmoplasia
Fibrous tissue formation in response to neoplasm
Most commonly mutated proto-oncogene in human cancers
RAS