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(A) Nodular sclerosing common Hodgkin’s lymphoma (NS-CHL): the normal lymph node structure is largely effaced because of a nodular growth; the nodule is surrounded by thick collagen bands originating from the capsule (haematoxylin and eosin; original magnification, × 40). Inset: birefringence of collagen bands (polarised light microscopy; original magnification, × 20). (B) NS-CHL: scattered lacunar cells can easily be seen within one nodule (haematoxylin and eosin; original magnification, × 300). Inset: cytological details of a lacunar cell (Giemsa; original magnification, × 800). (C) NS-CHL: so called cellular phase; note the nodularity of the growth (haematoxylin and eosin; original magnification, × 80). (D) NS-CHL: so called syncytial variant; note the cohesive growth pattern of neoplastic cells (haematoxylin and eosin; original magnification, × 400). (E) NS-CHL: an example of grade II tumour; note the content of neoplastic cells within the nodule, which covers more than 25% of the examined area (haematoxylin and eosin; original magnification, × 300). (F) An example of anaplastic large cell lymphoma of the Hodgkin-like type (ALCL-HL): the tumour consists of nodules partly surrounded by collagen bands (haematoxylin and eosin, original magnification, × 20).(G) ALCL-HL: at higher magnification it can be seen that the collagen bands are almost exclusively formed by neoplastic cells (Giemsa; original magnification, × 300). (H) ALCL-HL: typical intrasinusoidal diffusion of neoplastic cells as shown by CD30 staining (APAAP technique, Gill’s haematoxylin counterstain; original magnification, × 200). (I) ALCL-HL: ALK protein expression by neoplastic cells (APAAP technique, Gill’s haematoxylin counterstain; original magnification, × 400). (J) Primary mediastinal large B cell lymphoma (PMLBCL): neoplastic cells sometimes have multiple nuclei, show a wide rim of clear, fragile cytoplasm, and elicit a stromal reaction with compartmentalisation (Giemsa; original magnification, × 300). (K) PMLBCL: neoplastic cells express the CD30 molecule (APAAP technique, Gill’s haematoxylin counterstain; original magnification, × 300). (L) Mixed cellularity common Hodgkin’s lymphoma (MC-CHL): Hodgkin and Reed-Sternberg (H&RS) cells are easily identified; they are found with a cellular milieu consisting of small lymphocytes, some plasma cells, histiocytes, and granulocytes (haematoxylin and eosin; original magnification, × 350). (M) MC-CHL: an example of a mummified cell (arrow) (haematoxylin and eosin; original magnification, × 350). 

(A) Nodular sclerosing common Hodgkin’s lymphoma (NS-CHL): the normal lymph node structure is largely effaced because of a nodular growth; the nodule is surrounded by thick collagen bands originating from the capsule (haematoxylin and eosin; original magnification, × 40). Inset: birefringence of collagen bands (polarised light microscopy; original magnification, × 20). (B) NS-CHL: scattered lacunar cells can easily be seen within one nodule (haematoxylin and eosin; original magnification, × 300). Inset: cytological details of a lacunar cell (Giemsa; original magnification, × 800). (C) NS-CHL: so called cellular phase; note the nodularity of the growth (haematoxylin and eosin; original magnification, × 80). (D) NS-CHL: so called syncytial variant; note the cohesive growth pattern of neoplastic cells (haematoxylin and eosin; original magnification, × 400). (E) NS-CHL: an example of grade II tumour; note the content of neoplastic cells within the nodule, which covers more than 25% of the examined area (haematoxylin and eosin; original magnification, × 300). (F) An example of anaplastic large cell lymphoma of the Hodgkin-like type (ALCL-HL): the tumour consists of nodules partly surrounded by collagen bands (haematoxylin and eosin, original magnification, × 20).(G) ALCL-HL: at higher magnification it can be seen that the collagen bands are almost exclusively formed by neoplastic cells (Giemsa; original magnification, × 300). (H) ALCL-HL: typical intrasinusoidal diffusion of neoplastic cells as shown by CD30 staining (APAAP technique, Gill’s haematoxylin counterstain; original magnification, × 200). (I) ALCL-HL: ALK protein expression by neoplastic cells (APAAP technique, Gill’s haematoxylin counterstain; original magnification, × 400). (J) Primary mediastinal large B cell lymphoma (PMLBCL): neoplastic cells sometimes have multiple nuclei, show a wide rim of clear, fragile cytoplasm, and elicit a stromal reaction with compartmentalisation (Giemsa; original magnification, × 300). (K) PMLBCL: neoplastic cells express the CD30 molecule (APAAP technique, Gill’s haematoxylin counterstain; original magnification, × 300). (L) Mixed cellularity common Hodgkin’s lymphoma (MC-CHL): Hodgkin and Reed-Sternberg (H&RS) cells are easily identified; they are found with a cellular milieu consisting of small lymphocytes, some plasma cells, histiocytes, and granulocytes (haematoxylin and eosin; original magnification, × 350). (M) MC-CHL: an example of a mummified cell (arrow) (haematoxylin and eosin; original magnification, × 350). 

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Despite its well known histological and clinical features, Hodgkin's lymphoma (HL) has recently been the object of intense research activity, leading to a better understanding of its phenotype, molecular characteristics, histogenesis, and possible mechanisms of lymphomagenesis. There is complete consensus on the B cell derivation of the tumour in m...

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... However, when they take on a multinucleated form, they are termed Reed-Sternberg cells. The presence and characteristics of Hodgkin and Reed-Sternberg cells play a pivotal role in diagnosing and understanding the disease's progression [23]. On the other hand, non-Hodgkin Lymphoma is more common and encompasses various lymphoma types originating from different lymphocytes. ...
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Biotechnology is one of the emerging fields that can add new and better application in a wide range of sectors like health care, service sector, agriculture, and processing industry to name some. This book will provide an excellent opportunity to focus on recent developments in the frontier areas of Biotechnology and establish new collaborations in these areas. The book will highlight multidisciplinary perspectives to interested biotechnologists, microbiologists, pharmaceutical experts, bioprocess engineers, agronomists, medical professionals, sustainability researchers and academicians. This technical publication will provide a platform for potential knowledge exhibition on recent trends, theories and practices in the field of Biotechnology
... Hodgkin lymphoma (HL; formerly called Hodgkin's disease) is a germinal center, B-cell malignant disorder that affects the reticuloendothelial and lymphatic systems (1). ...
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Background The incidence of Hodgkin’s lymphoma (HL) in HIV-positive individuals is approximately 19X more than in HIV-negative persons. Most HIV-HL patients present at an advanced stage (Ann Arbor stage III-IV), have “B” symptoms and extranodal involvement. HAART's development has led to a significant change in the natural history and risk stratification of HIV-HL. Therefore, this study aimed to determine differences in clinicopathological and survival patterns of HL among individuals with and without HIV disease in Tanzania in the HAART era. Methodology This hospital-based retrospective cohort study was conducted at the ORCI, Dar-Es-Salaam, Tanzania. Chi-square and Fisher’s exact tests were used to compare proportions. Student t-test was used to compare means. The log-rank test was applied to the variables in univariate analysis to identify factors that predict survival. The factors that were significant in univariate analysis were then analyzed in multivariate fashion using a Cox regression model. Results 83 patients with HL were recruited, and the prevalence of HIV-positive status was 27.7%. Most of the patients with HIV-HL had an age of more than 30 years (73.9%), while most of the non-HIV-HL patients had an age of less than 30 years (63.3%) (P = 0.02). The 2-year OS rate for HIV-HL was 34%, while that for non-HIV-HL was 67%. Among the HIV-HL patients, predictors of a poorer outcome were a CD4 count ≤ 200 cells/mm3 (P = 0.05), lack of HAART use (P = 0.00), and the use of HAART for ≤ 10 months (P = 0.00). Conclusion The prevalence of HIV-HL was 27.7% among HL patients. HIV positivity is still a poor prognostic factor in our setting, especially for patients not on HAART, on HAART for less than ten or ten months, or with a low CD4 count below 200 cells/mm3.Patients with HIV-HL were older and had higher LDH levels, whereas patients with non-HIV-HL were younger and had low LDH levels.
... Despite advances in medical imaging technology, it is difficult for even experienced hematopathologists to identify different subtypes of lymphoma. Diagnosis of lymphoma is firstly based on the pattern of growth and the cytologic features of the abnormal cells, then clinical, molecular pathology, immunohistochemical, and genomic features are required to finalize the identification of certain subtypes [6]. However, clinical routine methods that enable tissue-specific diagnosis, such as image-guided tumor biopsy and percutaneous needle aspiration, have the shortcomings of subjectivity, costly, and poor classification accuracy [7]. ...
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... 35 CD30 is a major marker of HRS cells and its expression occurs in >95% of cases of cHL. 36,37 Signal transduction through CD30 leads to the activation of NF-kB and mitogen-activated protein kinase (MAPK) pathways, resulting in proliferative and anti-apoptotic effects in HRS cells. 38 At the same time, under physiological conditions, CD30 expression is found on minor subpopulations of activated B lymphocytes, and NK cells, as well as on 3%-31% of circulating T lymphocytes. ...
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... In addition to morphological differences, B lymphocytes express specific surface markers including CD19, CD20, and CD21. These markers were used to identify and differentiate the cell population [45,46]. ...
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