2016-10-19T22-45-34Z
Source: International Journal of Medical Science and Public Health
Ravi G Patel, Pooja Y Shah, Shridhan G Prajapati, Nirali S Amin, Varsha S Khant.
Background: Round Cell Tumors are heterogeneous malignancy featuring primitive undifferentiated small cell morphology. Small round cell tumors mostly occur in children, adolescents, and young adults. Because of their significant morphological overlap, have become a paradigm for an integrated approach to diagnosis. Immunohistochemistry (IHC) is the most common ancillary technique used for differential diagnosis of round cell tumors. Finding from all these studies are reviewed and interpreted in respect with clinical history, laboratory investigations, and diagnostic imaging finding. Objectives: (i) To study the incidence, and age vs. sex wise distribution of round cell tumors. (ii) To study the Immunohistochemical (IHC) pattern of these different round cell tumors and correlate the morphological diagnosis with IHC to determine its role as a confirmatory or diagnostic marker of the round cell tumors. Materials and Methods: As a part of study 75 (seventy-five) cases were selected during the year 2013-2015. Relevant findings were obtained. Biopsy tissues/ samples were fixed, paraffin embedded, sectioned and, stained with hematoxylin and eosin. IHC was performed on each case. Results were analyzed and compared. Results: Out of 75 cases, there were 22 cases (29.33%) of Non-Hodgkins lymphoma with the highest incidence. According to age wise distribution, the highest incidence was observed in 0-10 years of age group. According to sex wise distribution, a higher incidence was observed in males. There were 50 cases (66.66 %) of Males and 25 cases (33.33%) of Females. Overall M:F ratio was 2:1. Based on IHC, 22 cases of NHL were further classified into Burkitts lymphoma, Lymphoblastic lymphoma, and Diffuse Large B-cell lymphoma. IHC study of PNET and Rhabdomyosarcoma showed CD 99(86.7%), NSE(73.3%) and Vimentin(100%) positivity and Desmin, Actin, CD 99 and Vimentin positivity respectively. IHC study of Neuroblastoma and medulloblastoma showed NSE, NF, Chromogranin, S 100 and Synaptophysin positivity and GFAP, Synaptophysin, Vimentin, and Ki67 positivity respectively. Conclusion: Most frequent Round Cell Tumors are Non-Hodgkins Lymphoma, Neuroblastoma, Ewing/PNET and Rhabdomyosarcoma. Neuroblastoma, Retinoblastoma, Wilms Tumor, Hepatoblastoma show presentation in early childhood while Rhabdomyosarcoma is seen throughout childhood. The majority of round cells tumors have male predominance. This study emphasizes the role of immunohistochemistry (IHC) to arrive a definite diagnosis.
http://ift.tt/2dpio58
Τετάρτη 19 Οκτωβρίου 2016
Histopathological study of Round Cell tumors - A retrospective study
Εγγραφή σε:
Σχόλια ανάρτησης (Atom)
Δημοφιλείς αναρτήσεις
-
from #AlexandrosSfakianakis via Alexandros G.Sfakianakis on Inoreader http://ift.tt/2jCvX3K via IFTTT
-
Abstract Purpose of Review Our goal is to summarize the airway disease literature since September 11, 2001 (9/11), focusing on studies pub...
-
Treatment effectiveness holds considerable importance in the association between service quality and satisfaction in medical service studies...
-
Vol.25 No.2 from #AlexandrosSfakianakis via Alexandros G.Sfakianakis on Inoreader http://ift.tt/1P7bHxT via IFTTT
-
Publication date: Available online 16 January 2017 Source: International Journal of Pediatric Otorhinolaryngology Author(s): Kaveh Karimn...
-
Understanding Head And Neck Cancers - The Southeast Sun ... The Southeast Sun (NAPSI)—According to the Centers for Disease Control an...
-
Abstract Background Henoch–Schönlein purpura is the most common vasculitis in children. Its long-term prognosis depends on renal involve...
-
Publication date: 21 February 2017 Source: Cell Reports, Volume 18, Issue 8 Author(s): Arielle Glatman Zaretsky, Christoph Konradt, Fabien...
-
Publication date: September 2017 Source: International Journal of Biological Macromolecules, Volume 102 Author(s): Mohamed Esmat, Ahmed A...
Δεν υπάρχουν σχόλια:
Δημοσίευση σχολίου