C. Perniciaro et al., SUBCUTANEOUS T-CELL LYMPHOMA - REPORT OF 2 ADDITIONAL CASES AND FURTHER OBSERVATIONS, Archives of dermatology, 129(9), 1993, pp. 1171-1176
Background: Peripheral T-cell lymphomas involving subcutaneous tissue
are rare. With modern immunohistochemical stains, subcutaneous T-cell
lymphomas may be demonstrated in patients previously thought to have f
atal Weber-Christian disease, malignant histiocytosis, and histiocytic
cytophagic panniculitis. Observations: We describe two young women wi
th subcutaneous lymphomas. They presented with erythematous nodular le
sions, which suggested benign panniculitis. Skin biopsy specimens in b
oth patients demonstrated large atypical lymphocytes in the subcutaneo
us tissue, karyorrhexis, and cytophagia. Immunohistochemical studies c
onfirmed a T-cell phenotype. Molecular genetics studies performed in o
ne patient showed a major T-cell clonal population. Conclusions: Subcu
taneous T-cell lymphoma is a rare, distinct subtype of postthymic peri
pheral T-cell lymphoma. Cytophagic ''histiocytic'' panniculitis is fre
quently a prominent histologic feature. Early systemic chemotherapy ma
y offer therapeutic advantages in patients with this disease.