Non-Hodgkin’s Lymphoma in Northern India: An Analysis of Clinical Features of 241 Cases
CC BY-NC-ND 4.0 ? Indian J Med Paediatr Oncol 2018; 39(01): 42-45
DOI: DOI: 10.4103/ijmpo.ijmpo_36_17
Abstract
Background: Geographic variations with regard to incidence, clinical presentation, and histological subtypes are known to occur in several cancers. This study was aimed to see if similar differences existed in non-Hodgkin's lymphoma (NHL) also during pre-immunohistochemical era. Materials and Methods: Cases of NHL seen at Institute Rotary Cancer Hospital, All India Institute of Medical Sciences, New Delhi from January 1997 to December 2000, were analyzed for baseline clinical features and histology. Results: Total cases: 241, median age: 47 years (range 2-84 years), male-female ratio: 2.2:1, primary extranodal NHL: 44.2%, the most common histological subtype: Diffuse large cell (6.2% of the cases).?Conclusion:?Our patients presented at younger median age, had more male to female ratio, had diffuse large cell histology as the most common histological subtype.
Keywords
Extranodal non-Hodgkin's lymphoma - non-Hodgkin's lymphoma - Northern India
Publication History
23 June 2021 (online)
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India
Abstract
Background: Geographic variations with regard to incidence, clinical presentation, and histological subtypes are known to occur in several cancers. This study was aimed to see if similar differences existed in non-Hodgkin's lymphoma (NHL) also during pre-immunohistochemical era. Materials and Methods: Cases of NHL seen at Institute Rotary Cancer Hospital, All India Institute of Medical Sciences, New Delhi from January 1997 to December 2000, were analyzed for baseline clinical features and histology. Results: Total cases: 241, median age: 47 years (range 2-84 years), male-female ratio: 2.2:1, primary extranodal NHL: 44.2%, the most common histological subtype: Diffuse large cell (6.2% of the cases).?Conclusion:?Our patients presented at younger median age, had more male to female ratio, had diffuse large cell histology as the most common histological subtype.
Keywords
Extranodal non-Hodgkin's lymphoma - non-Hodgkin's lymphoma - Northern India
Introduction
The incidence of non-Hodgkin's lymphoma (NHL) is rising worldwide. In addition, geographic variations in its incidence and clinical behavior are well known.[1] NHL despite being the most common lympho-hematopoietic malignancy in India, has lower age-standardized incidence rate (ASR) (0.8?5.1 males, 0.6?3.1 females) than that seen in the USA (16.1 males and 10.8 females). Low-grade NHL (follicular lymphoma, and chronic lymphocytic leukemia) is more common in the USA, whereas diffuse large B cell lymphoma is more common in India, Burkitt's lymphoma occurs more frequently in tropical Africa, Immunoproliferative small intestinal disease in the Middle East and adult T-cell leukemia/lymphoma in South West Japan and the Caribbean basin.[1],[2],[3],[4] Despite being a large country publications for NHL from India in general and northern India, in particular, are limited. The subclassification of NHL has gone substantial changes with the availability of new immunohistochemical markers, and also the availability of monoclonal antibody (anti-CD 20 antibody) has changed the treatment outcome of B-cell lymphoma,[1] but this study predates these or when these parameters or treatment options were not freely available to our patients and diagnosis was based mainly on morphology. Hence, we decided to analyze the clinical features of NHL seen at our center.
Materials and Methods
Patients of NHL registered at Institute Rotary Cancer Hospital (IRCH), All India Institute of Medical Sciences (AIIMS) between January 1, 1997 and December 31, 2000 were included in this study. The IRCH files of the patients were taken from the record section and scrutinized for the epidemiological, clinical, and laboratory data. Confirmation of the histopathological diagnosis at AIIMS was mandatory for inclusion in the study. Other inclusion criteria were treatment naive and those who received treatment at AIIMS. Patients with fine-needle aspiration cytology based diagnosis were excluded.
Working formulation classification of NHL was used for classification.[4] Ann Arbor classification was used to staging the patients.[5] The stage at initial presentation was determined on the basis of clinical, radiological, and laboratory data available in the files.
Results
Of the 241 patients included in the study, 168 were male and 73 were female with a male to female ratio of 2.2:1. The median age at presentation was 47 years, range 2?84 years. ?B? symptoms were present in 104 patients (43.2%).
One hundred and sixty-seven patients (69.3%) had peripheral lymphadenopathy, whereas 107 (44.4%) had axial lymphadenopathy [Table 1]. It was generalized (involvement of 3 or more noncontiguous lymph node areas) in 54 cases (22.4%). Individual sites of lymphadenopathy are shown in [Table 1]. Bulky lymphadenopathy was seen in 41 patients (17%) and superior vena cava syndrome in 4 (1.7%) at presentation.
Clinical Characteristic |
Clinical details |
---|---|
*SVC features ? Superior vena cava obstruction features |
|
Age |
Median 47 years (range 2-84) |
Sex |
Male 168, female 73, male female ratio - 2.2:1 |
Symptom duration |
Median 4 months (range 0.5-6.0) |
?B? symptoms |
104 patients (43.2%) |
Peripheral |
167 patients (69.3%), generalized - 54, |
lymphadenopathy |
cervical - 138, axillary - 34, epitrochlear - 6, inguinal - 34 |
Axial lymphadenopathy |
107 patients (44.4%), mediastinal - 22, hilar - 14, retroperitoneal - 77, coeliac - 11, portahepatic - 9, mesenteric - 22, iliac - 16 |
Bulky lymphadenopathy |
41 patients (17%) |
SVC features* |
4 patients (1.7%) |
Malignant cell positive pleural effusion |
19 patients (3%) |
Malignant cell positive ascites |
22 patients (4%) |
Extra nodal site |
Number of cases |
---|---|
Head and neck region |
53 cases (22%), tonsil - 23, sino nasal tract - 6, nasopharynx - 12, oropharynx - 1, orbit - 9, parotid - 1, thyroid - 2 |
Gastro intestinal region |
29 cases (12%), stomach - 17, small intestine - 4, colon - 5, ileocaecal region - 2, rectum - 1 |
Other sites |
Brain - 4, spine - 4, bone - 5, skin - 6, testis - 3, urinary bladder - 2 |
Histological subtype |
Number of patients (%) |
---|---|
*Others include MALT lymphoma (2 cases), AILD lymphoma (1 case), Primary cutaneous T-cell lymphoma (1 case), Mycosis fungoides (2 cases) and unspecified (25 cases). MALT ? Mucosa associated lymphoid tissue; AILD ? Angio immunoblastic lymphadenopathy with dysproteinemia |
|
Small lymphocytic lymphoma |
6 (2.48) |
Follicular small cleaved cell |
15 (6.22) |
Follicular mixed small cleaved and large cell |
5 (2.07) |
Follicular large cell |
1 (0.41) |
Diffuse small cleaved cell |
11 (4.56) |
Diffuse mixed small cleaved and large cell |
11 (4.56) |
Diffuse large cell |
146 (60.58) |
Large cell immunoblastic |
3 (1.24) |
Lymphoblastic |
9 (3.73) |
Small noncleaved cell |
3 (1.24) |
Others* |
31 (12.86) |
Stage |
Number of patients (%) |
---|---|
I |
55 (22.82) |
II |
57 (23.65) |
III |
45 (18.67) |
IV |
84 (34.85) |
Site of involvement |
Number of patients (%) |
---|---|
Bone marrow |
53 (63.09) |
Liver |
9 (10.71) |
Malignant cell positive ascites |
4 (4.76) |
Malignant cell positive pleural effusion |
3 (3.57) |
Multiple extra nodal sites |
6 (7.14) |
Multi focal bone involvement |
1 (119) |
Brain |
4 (4.76) |
Spine |
4 (4.76) |
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