Lymphocytic predominant Hodgkin's disease or type I Hodgkin's disease (paragranuloma of Poppema-Lennert): a clinicopathological entity. Study of 21 cases and review of the literature
V. Meignin et al., Lymphocytic predominant Hodgkin's disease or type I Hodgkin's disease (paragranuloma of Poppema-Lennert): a clinicopathological entity. Study of 21 cases and review of the literature, ANN PATHOL, 20(1), 2000, pp. 19-24
We have studied clinical and pathological features of a series of 21 patien
ts followed at the hospital Saint-Louis for a nodal nodular lymphocytic pre
dominant Hodgkin's disease or para-granuloma of Poppema-Lennert. Histopatho
logically, all these lymph nodes were involved by a nodular proliferation o
f atypical cells, called << pop corn >> cells with a B cell phenotype, admi
xed with small lymphocytes. Clinically, most patients were young males. The
disease was localized except in one case and the prognosis good (only one
death). However, one patient relapsed and another developped an aggressive
lymphoma. These results were in keeping with different studies in the liter
ature and confirmed that the paragranuloma is a clinicopathological entity,
distinct from the classical Hodgkin's disease. Nowadays, it's strongly sug
gested that the << pop corn >> cell is of centroblastic origin. Treatment r
emains controversial, however, according to most of the authors, patients w
ith localized disease could be followed without treatment after surgical ex
cision.