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. Author manuscript; available in PMC: 2020 Oct 23.
Published in final edited form as: Histopathology. 2017 Dec 4;72(4):588–600. doi: 10.1111/his.13395

Table 2:

SDH-Deficient RCC

Case Age/Sex Size/Stage Notable pathologic features Clinical history
SDH #1 21/F 6 cm
pT1Nx
Nested, vacuolated cytoplasm, rare inclusions NED x 61 months, no h/o neoplasia or genetic syndrome
SDH #2 17/M 9.1 cm
pT2Nx
Tubular with focal papillary architecture.
Called oncocytoma on frozen section.
Presented with hypertension.
No f/u available
SDH #3 20/M 7.4 cm
pT2Nx
Vacuolated with inclusions No f/u available
SDH #4 19/M Size unknown Nested with vacuolated cytoplasm and rare inclusions NED x 11 months, no h/o neoplasia or genetic syndrome
SDH #5 31/M 15 cm
pT2N0
Pleomorphic, vacuolated, t(6:11)-like No f/u available
SDH #6 17/M 6.5 cm
pT1Nx
t(6;11)-like Presented with hematuria.
No f/u available
SDH #7 22/F 9.0 cm
pT2Nx
Vacuolated cytoplasm No f/u available
SDH #8 34/M 10 cm
pT2NxMx
Pleomorphic with necrosis T12 bone metastasis at diagnosis

f/u= follow-up; h/o= history of; NED= no evidence of disease