Skip Navigation
Skip to contents

J Pathol Transl Med : Journal of Pathology and Translational Medicine

OPEN ACCESS
SEARCH
Search

Search

Page Path
HOME > Search
2 "Diagnosis, Differential"
Filter
Filter
Article category
Keywords
Publication year
Authors
Original Articles
Use of Calretinin, CD56, and CD34 for Differential Diagnosis of Schwannoma and Neurofibroma.
Ji Young Park, Hoon Park, Nam Jo Park, June Sik Park, Hyun Jung Sung, Sang Sook Lee
Korean J Pathol. 2011;45(1):30-35.
DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.1.30
  • 4,675 View
  • 106 Download
  • 15 Crossref
AbstractAbstract PDF
BACKGROUND
It is important to differentiate between schwannomas and neurofibromas for the cases in which the histopathologic features overlap. Depending on the tumor type, surgeons can decide on a treatment method and whether to preserve or sacrifice the nerve; the possibility of malignant transformation in the case of neurofibromas also needs to be considered.
METHODS
We studied 101 cases of schwannoma and 103 cases of neurofibroma. All the hematoxylin and eosin slides for these cases were reviewed, and tissue microarrays were prepared from the representative areas. Immunohistochemical analysis was performed using antibodies for S-100 protein, calretinin, CD56 and CD34.
RESULTS
All the tumors except 3 neurofibromas were positive for the S-100 protein. Calretinin was found in 26.7% of the schwannomas (27/101), but it was not found in any of the neurofibromas. CD56 was positive in 77.2% of the schwannomas (78/101) and in 9.8% of the neurofibromas (10/102). CD34 was positive in 42.5% of the schwannomas (43/101) and in 80.2% of the neurofibromas (81/101). Statistically, calretinin was significantly specific for schwannomas (p<0.001) and CD56 was also sensitive for these tumors (p<0.001). On the other hand, a CD34 expression seemed highly sensitive (p<0.001) for neurofibromas.
CONCLUSIONS
We concluded that combined immunohistochemical analysis for calretinin, CD56, and CD34 may be very useful for differentiating schwannomas from neurofibromas.

Citations

Citations to this article as recorded by  
  • Ancient cervical vagal schwannoma and an interposition great auricular to vagus nerve graft
    Nicholas Figaro, Rickhi Ramoutar, David Richards, Rodolfo Arozarena, Mala Geelal, Solaiman Juman
    Edorium Journal of Otolaryngology.2024; 5(2): 1.     CrossRef
  • Lung schwannomas, an unusual entity
    Nazia M. Walvir, Rumana H. Makhdoomi, Meesa Zargar, Aiffa Aiman, Shadab Maqsood
    Lung India.2023; 40(1): 70.     CrossRef
  • A Spectrum of Histomorphological and Immunohistochemical Expression Profiles of S-100, CD56 and Calretinin in Benign Peripheral Nerve Sheath Tumours
    Poornima Jaiswal, Anand CD, Jaison Jacob John
    Cureus.2023;[Epub]     CrossRef
  • An unusual diffuse CD34 staining in an olfactory groove cellular schwannoma: Case report
    Marios Theologou, Jorge D. Perez Ruiz, Panagiotis Varoutis, Nicolaos Flaris, Nikolaos `Skoulios
    Archivos de Neurociencias.2023;[Epub]     CrossRef
  • An unusual diffuse CD34 staining in an olfactory groove cellular schwannoma: Case report
    Marios Theologou, Jorge D. Perez Ruiz, Panagiotis Varoutis, Nicolaos Flaris, Nikolaos `Skoulios
    Archivos de Neurociencias.2023;[Epub]     CrossRef
  • Intranodal Neurofibroma: A Case Report and Literature Review
    Steven H. Adams, Tara L. Huston, Daniel Lozeau
    The American Journal of Dermatopathology.2022; 44(4): 306.     CrossRef
  • A rare case of pseudoglandular schwannoma
    Fadime Eda GÖKALP SATICI, Hamide SAYAR
    Journal of Surgery and Medicine.2022; 6(4): 1.     CrossRef
  • Gastric Schwannoma as an Important and Infrequent Differential Diagnosis of Gastric Mesenchymal Tumours: A Case Report and Review of Literature
    Abdalla Saad Abdalla Al-Zawi, Salma Lahmadi, Saman Jalilzadeh Afshari, Ipshita Kak, Salem Alowami
    Cureus.2022;[Epub]     CrossRef
  • Spindle cell proliferations of the sigmoid colon, rectum and anus: a review with emphasis on perineurioma
    Patrice Grech, John B Schofield
    Histopathology.2020; 76(3): 342.     CrossRef
  • Large retroperitoneal schwannoma: a rare cause of chronic back pain
    Milan Radojkovic, Dragan Mihailovic, Miroslav Stojanovic, Danijela Radojković
    Journal of International Medical Research.2018; 46(8): 3404.     CrossRef
  • Nasal Septal Schwannoma
    Hyun Jin Min, Seok Chan Hong, Kyung Soo Kim
    Journal of Craniofacial Surgery.2017; 28(1): e97.     CrossRef
  • Neurofibroma of the Colon: A Diagnostic Mimicker of Gastrointestinal Stromal Tumor
    Soomin Ahn, Choon Sik Chung, Kyoung-Mee Kim
    Case Reports in Gastroenterology.2016; 10(3): 674.     CrossRef
  • Solitary Epibulbar Neurofibroma in Older Adult Patients
    Thais Shiota Tanaka, Victor M. Elner, Hakan Demirci
    Cornea.2015; 34(4): 475.     CrossRef
  • Syncytial nuclear aggregates in normal placenta show increased nuclear condensation, but apoptosis and cytoskeletal redistribution are uncommon
    S.J. Coleman, L. Gerza, C.J.P. Jones, C.P. Sibley, J.D. Aplin, A.E.P. Heazell
    Placenta.2013; 34(5): 449.     CrossRef
  • Analysis of syncytial nuclear aggregates in preeclampsia shows increased sectioning artefacts and decreased inter-villous bridges compared to healthy placentas
    S.J. Calvert, C.J.P. Jones, C.P. Sibley, J.D. Aplin, A.E.P. Heazell
    Placenta.2013; 34(12): 1251.     CrossRef
Malignant Mesothelioma in Body Fluids: with Special Reference to Differential Diagnosis from Metastatic Adenocarcinoma.
Jin Ho Paik, Jin Haeng Chung, Baek Hui Kim, Gheeyoung Choe
Korean J Pathol. 2009;43(5):458-466.
DOI: https://doi.org/10.4132/KoreanJPathol.2009.43.5.458
  • 3,389 View
  • 32 Download
AbstractAbstract PDF
BACKGROUND
Malignant mesothelioma (MM) is a rare malignant neoplasm occurring in pleura, pericardium, and peritoneum. The differential diagnosis between MM and metastatic adenocarcinoma (MA) causes diagnostic, staging, and therapeutic dilemmas. Herein, we investigated characteristic cytologic features of MM.
METHODS
Cytologic specimens of MM (n=10), MA (n=25), and reactive mesothelial hyperplasia (n=10) were retrieved and reviewed from archival materials in the Department of Pathology, Seoul National University Bundang Hospital from May 2003 to July 2008.
RESULTS
MM showed tumor cell clusters and singly scattered malignant tumor cells forming single cell populations with sparse reactive benign mesothelial cells. In contrast, MA showed distinct two cell populations of tumor cell clusters and scattered reactive mesothelial cells. Furthermore, MM frequently exhibited a characteristic long chain-like arrangement (hand-in-hand appearance) and intercellular windows, which were rarely evident in MA. Variable nuclear size, relatively consistent nuclear-cytoplasmic ratio, bior multi-nucleation, and lacy cytoplasmic borders were also frequently observed in MM.
CONCLUSIONS
Differential diagnosis of MM from MA in body fluids is possible based on meticulous examination of certain cytologic parameters, which could have significant implications in staging and treatment.

J Pathol Transl Med : Journal of Pathology and Translational Medicine
TOP