Nodular lymphoid hyperplasia of the small intestine and malignant lymphoma

1981 ◽  
Vol 26 (9) ◽  
pp. 860-861
Author(s):  
C. Matuchansky ◽  
M. Morichau-Beauchant
1985 ◽  
Vol 313 (3) ◽  
pp. 166-171 ◽  
Author(s):  
Claude Matuchansky ◽  
Guy Touchard ◽  
Marc Lemaire ◽  
Philippe Babin ◽  
François Demeocq ◽  
...  

Blood ◽  
1974 ◽  
Vol 43 (3) ◽  
pp. 389-400 ◽  
Author(s):  
Arkadi M. Rywlin ◽  
Rolando S. Ortega ◽  
Carlos J. Dominguez

Abstract A study of consecutive bone marrow aspirates from 365 patients without lymphoproliferative disorder, ten patients with chronic lymphocytic leukemia (CLL), and 25 patients with malignant lymphoma disclosed a clear separation of normal from abnormal lymphoid nodules (LN). Normal LN were found in 47% of patients and were classified into lymphoid follicles and lymphoid infiltrates. A new entity, nodular lymphoid hyperplasia (NLH), was diagnosed on ten bone marrows which contained a low-power field displaying four or more lymphoid nodules or showed a lymphoid nodule larger than 0.6 mm. The clinical significance of nodular lymphoid hyperplasia remains unknown; in certain cases it represents a precursor state of a mature lymphocytic lymphoproliferative disorder. Nodular aggregates in CLL are of the infiltrate type and exhibit a tendency to confluence. Eleven of the 25 patients with malignant lymphoma displayed lymphoreticular nodules which were cytologically similar to the original lymphoma and different from normal LN. Two patients, one with reticulum cell sarcoma and one with Hodgkin’s disease, showed NLH of the bone marrow. Bone marrow LN in patients with an established diagnosis of mature lymphocytic lymphoma have to be interpreted with the utmost caution. Confluence of LN, irregular shapes, and the presence of prolymphocytes and lymphoblasts speak for lymphomatous nodules. Additional clinicopathologic studies are necessary to sharpen the distinction between NLH and well-differentiated lymphoproliferative disorders.


1966 ◽  
Vol 40 (1) ◽  
pp. 78-89 ◽  
Author(s):  
Paul E. Hermans ◽  
Kenneth A. Huizenga ◽  
Harry N. Hoffman ◽  
Arnold L. Brown ◽  
Harold Markowitz

PEDIATRICS ◽  
1968 ◽  
Vol 42 (5) ◽  
pp. 833-837
Author(s):  
Joyce D. Gryboski ◽  
Thomas W. Self ◽  
Arthur Clemett ◽  
Teodoro Herskovic

A 13-year-old boy with chronic diarrhea and abdominal pain since 6 months of age, and recurrent fevers since 12% years of age, was found to have deficiency of IgA and nodular lymphoid hyperplasia of the small intestine. This disorder was similar to that of "dysgammaglobulinemia and intestinal lymphoid hyperplasia" described in adults in 1966. An associated giardiasis was eliminated by atabrine therapy and a malabsorption syndrome, cleared after treatment with tetracycline. Diarrhea and abdominal pain were not alleviated until he was treated with monthly fresh frozen plasma infusions. It is to be emphasized that other forms of chronic diarrhea not related to immunoglobuun deficiencies do not respond to this type of therapy.


1980 ◽  
Vol 25 (7) ◽  
pp. 553-557 ◽  
Author(s):  
Cornelis B. H. W. Lamers ◽  
D. J. Theo Wagener ◽  
Karel J. M. Assmann ◽  
Jan H. M. Van Tongeren

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