Xincen Duan, Ph.D., Minglong Zhang, M.Sc., Yan Liu, Ph.D., Wenbo Zheng, Ph.D., Chun Yee Lim, Ph.D., Sollip Kim, Ph.D., Tze Ping Loh, M.B., BCh, BAO, Wei Guo, Ph.D., Rui Zhou, M.D., Ph.D., and Tony Badrick, Ph.D.; On behalf of the Patient-Based Real-Time Quality Control Working Group of the Asia Pacific Federation of Clinical Biochemistry and Laboratory Medicine. Ann Lab Med 2024;44:385-91. https://doi.org/10.3343/alm.2024.0053
Jiwon You, M.S., Hyeon Seok Seok, B.S.E., Sollip Kim, M.D., Ph.D., and Hangsik Shin, Ph.D.. Ann Lab Med -0001;0:. https://doi.org/10.3343/alm.2024.0354
1 July 2010 in Applied Immunohistochemistry & Molecular Morphology
Neuroblastoma is one of the most common solid tumors occurring in childhood. Bone marrow evaluation is an important part of clinical staging in neuroblastoma patients. In view of the difficulty of detecting neuroblastoma cells with conventional bone marrow aspirate smears and biopsy (BMB) and specimens in cases in which metastasis is not prominent, we propose the use of immunohistochemistry (IHC) as a potential diagnostic tool. We examined 116 BMB and 115 bone marrow clot (BMC) specimens from 60 newly diagnosed neuroblastoma patients for tumor cells. Neuroendocrine IHC markers, such as CD56, chromogranin A, and synaptophysin were applied to diagnose neuroblastoma. Eighteen out of the 60 patients (25.4%) displayed BM metastasis, as observed with conventional hematoxylin and eosin staining. IHC staining of BMC sections was generally more sensitive than that of BMB sections for tumor cell detection. We detected tumors in 5 and 7 additional hematoxylin and eosin-negative BMB and BMC sections, respectively, using CD56. Overall, CD56 or a combination of CD56 and chromogranin A was effective in detecting neuroblastoma cells. IHC analysis of BMB and BMC sections is warranted as a routine component of the diagnostic work-up of neuroblastoma to overcome discrepancies between routine smears and IHC stains.