scholarly journals Cytology and colchicine sensitivity of viable cells from lymph nodes with malignant lymphoma

Cancer ◽  
1978 ◽  
Vol 41 (5) ◽  
pp. 1845-1856 ◽  
Author(s):  
Robert Schrek ◽  
Zelma Molnar ◽  
Stefano S. Stefani
2021 ◽  
Author(s):  
Shu Kobayashi ◽  
Hideo Fukuhara ◽  
Shnikuro Yamamoto ◽  
Takashi Karashima ◽  
Mitsuko Iguchi ◽  
...  

2003 ◽  
Vol 127 (1) ◽  
pp. 60-63 ◽  
Author(s):  
James A. Strauchen ◽  
Lorraine K. Miller

Abstract Context.—The etiology of lymph node infarction may be difficult or impossible to determine by histologic examination. Lymph node infarction is followed by malignant lymphoma in some but not all patients. The role of immunohistochemistry in the evaluation of lymph node infarction is not well defined. Although it is widely believed that necrotic tissue is not suitable for immunohistochemical study, this view may be inaccurate. Objective.—To determine whether lymphoid antigens are preserved in infarcted lymph nodes and to determine the utility of immunohistochemical staining in the evaluation of lymph node infarction. Design.—Retrospective immunohistochemical study of infarcted lymph nodes using archival formalin-fixed, paraffin-embedded tissue. Setting.—Academic medical center. Patients.—Eleven adult patients with lymph node infarction retrieved from pathology files. Main Outcome Measures.—Results of immunohistochemistry, diagnosis of lymphoma. Results.—Preservation of lymphoid antigens was observed in 4 of 6 cases of lymph node infarction associated with malignant lymphoma, including 3 of 5 cases of diffuse large B-cell lymphoma and 1 case of peripheral T-cell lymphoma. Nonspecific staining was not encountered. In 1 case, in which an infarcted lymph node showed a benign pattern of lymphoid antigen expression, lymphoma has not developed after 5 years. Conclusion.—Lymphoid antigens are frequently preserved in cases of lymph node infarction, and immunohistochemical study of infarcted lymph nodes may provide clinically useful information.


1998 ◽  
Vol 59 (6) ◽  
pp. 1592-1595 ◽  
Author(s):  
Hiroki IMAZU ◽  
Takahiko FUNABIKI ◽  
Masahiro OCHIAI ◽  
Yoichi SAKURAI ◽  
Teruya SUGITA ◽  
...  

1965 ◽  
Vol 2 (1) ◽  
pp. 68-94 ◽  
Author(s):  
Hilton A. Smith

About 1100 cases of malignant lymphoma were studied. Malignant lymphomas in cattle occur mostly at the older ages but they are by no means absent in the very young. Sex, breed and season of the year have little significance. Nearly all organs and tissues are susceptible to invasion, but some much more so than others, lymph nodes and heart being outstanding. Several histological types are described, as well as a relation to Hodgkin's disease. Reactions by eosinophils, plasma cells and other cells are described and an attempt made to evaluate them etiologically. Considerable evidence suggests that this neoplastic disease originates as an unsuccessful, generalized defensive reaction.


1974 ◽  
Vol 11 (1) ◽  
pp. 52-59 ◽  
Author(s):  
R. C. Page ◽  
L. Schectman ◽  
W. F. Ammons ◽  
L. Dillingham

A spontaneous hematopoietic neoplasm in a cotton-top marmoset (Saguinus oedipus) was characterized by perivascular infiltration and invasion of the liver, kidneys, adrenals, spleen, lymph nodes, bone marrow, and lungs by a pleomorphic primitive reticular cell. A significant fraction of the circulating white cells was of the same cell type. The disease was diagnosed as lymphosarcoma of the reticulum-cell type with features similar to viral-induced malignancy previously described.


1983 ◽  
Vol 17 (6) ◽  
pp. 460-462 ◽  
Author(s):  
Terry L. Schwinghammer ◽  
Denise L. Howrie

Various lymph node abnormalities have been associated with phenytoin therapy. Four distinct categories of lymphadenopathy have been described: lymphoid hyperplasia, pseudolymphoma, pseudo-pseudolymphoma, and lymphoma. These presentations vary from a benign symptom complex, with enlarged lymph nodes, that is reversible upon drug discontinuance to a true malignant lymphoma that is progressive and ultimately fatal. Benign lymph node hyperplasia and pseudolymphoma may result in erroneous diagnosis and treatment of malignant lymphoma if phenytoin-associated lymphadenopathy has not been considered. We describe a patient who developed enlarged inguinal lymph nodes while receiving chronic phenytoin therapy. An initial diagnosis of malignant lymphoma was made, and recurrent hospitalizations and treatment with cytotoxic drugs ensued. Repeat biopsy, as well as reexamination of the removed nodes, later revealed phenytoin-associated hyperplasia. Patients who develop enlarged lymph nodes while receiving phenytoin should be evaluated carefully so that phenytoin-induced lymphadenopathy may be differentiated from true malignant lymphoma and appropriate treatment may be given.


1987 ◽  
Vol 28 (3) ◽  
pp. 253-262 ◽  
Author(s):  
R. Nyman ◽  
S. Rehn ◽  
B. Glimelius ◽  
H. Hagberg ◽  
A. Hemmingsson ◽  
...  

Magnetic resonance imaging (MRI) was compared with chest radiography, computed tomography (CT) and ultrasonography (US) for demonstration of spleen and liver engagement and enlarged lymph nodes in patients with malignant lymphoma. The investigation comprised 24 patients with Hodgkin's disease (HD) and 39 with non-Hodgkin lymphoma (NHL). MRI demonstrated enlarged lymph nodes, distinctly separated from vessels, fat, muscle, liver and occasionally also pancreas without any contrast medium. The distinction between lymph nodes and spleen was, however, poor in the images. In the mediastinum, MRI was superior to chest radiography and had an accuracy similar to that of CT. In the abdomen and the pelvis MRI had slight advantages over CT in detection of enlarged lymph nodes. Compared with US the MRI results were similar in the abdomen and somewhat better in the pelvis. MRI and US were better than CT in revealing HD infiltrates in the spleen. Infiltration of NHL in the spleen was slightly better disclosed at US than at CT and MRI; most of the NHL infiltration, confirmed at histopathology, could, however, not be revealed with any of the modalities, except when the size of the spleen was considered. Regions in the spleen, displayed with low image intensity in the T2 weighted image, were most likely due to increased amount of fibrotic tissue in the lymphomatous lesions. Good demonstration of lymph nodes and lymphomatous lesions in the spleen with MRI required two sequences; one with short TR and TE (T1 weighted image) and one with long TR and TE (T2 weighted image).


Cancer ◽  
1969 ◽  
Vol 23 (5) ◽  
pp. 1061-1073 ◽  
Author(s):  
Robert Schrek ◽  
Henry Rappaport ◽  
Myron E. Rubnitz ◽  
Hau C. Kwaan

Blood ◽  
2008 ◽  
Vol 112 (11) ◽  
pp. 5275-5275
Author(s):  
Jie He ◽  
Rui-ping Li ◽  
Jian-hua Wang ◽  
Bao-An Chen

Abstract Objective: Malignant lymphoma (ML), Kikuchi-Fuljimoto disease (KFD) and L-forms Acid-fast bacillus infection (L-forms TB) usually affect the cervical lymph nodes. KFD and L-form TB are often confused with ML and take misdiagnosis and inappropriate treatment. The diagnosed of these diseases is on basis of an excision biopsy of affected lymph nodes. Methods: We analyzed 63 patients (including case diagnosed in our hospital) by clinical characteristic, laboratory, pathological morphology, histochemistry and immunohistochemistry. Results: Of 63 cases, 43 were ML, 17 were KFD and 3 were L-forms TB. In ML disease, 46% were male and 54% were female, mean age was 54 (11–82). 9% cases have persistent fever and associated with hepatosplenomegaly. In KFD, 47% were male and 53% were female, mean age was 26 (17–45). 59% cases with cervical hymphadenopath and no fever, 41% had painful, accompanied by fever. hepathosplenomegaly, occasionally leucopenia and lypadenopathy especially involving cervical region not responsive to antibiotic treatment. 29% lymph tissues were morphologically, and characterized by a necrosis in the cortical or paracortical areas of enlarged lymph node around the necrotic area. T lymphocytes were found and absence of granulocytes. 30% cases were mistaken to ML. L-forms TB disease, there were fever, clinical and histological were similar KFD and ML. 3 cases were misdiagnosis to ML or KFD. Laboratory analyses: PAM and PAS were positive, and anti acid test to found L-forms bacterium in tissues. Conclusions: Kikuchi-Fujimoto disease and L-forms Acid-Fast bacillus infection are easily confused histological and clinically with malignant lymphoma. Clinicians and pathologists must be aware of this condition. Although Malignant lymphoma, Kikuchi-Fujimoto disease and L-forms Acid-fast bacillus infection can be found any age, but should be considered for malignant lymphoma in older patients. Kikuchi-Fujimoto disease is predominantly a self-limiting disease of the young and most cases with fever, nodal biopsy showing fragmentation necrosis and karyorrhexis, not responsive to antibiotic treatment. In the L-forms Acid-fast bacillus infection, the PAM and PAS are positive, and have an effective antibiotic treatment.


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