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Tytuł pozycji:

Composite Neuroblastoma Metastatic to a Lymph Node: The Novel Histopathologic Diagnosis of a Unique Multiclonal Neoplasm.

Tytuł:
Composite Neuroblastoma Metastatic to a Lymph Node: The Novel Histopathologic Diagnosis of a Unique Multiclonal Neoplasm.
Autorzy:
Kurtz JL; Stanford University School of Medicine, Department of Pathology, Stanford, CA, USA.
Shimada H; Stanford University School of Medicine, Department of Pathology, Stanford, CA, USA.
Hazard FK; Stanford University School of Medicine, Department of Pathology, Stanford, CA, USA .
Źródło:
Annals of clinical and laboratory science [Ann Clin Lab Sci] 2021 Jul; Vol. 51 (4), pp. 573-579.
Typ publikacji:
Case Reports; Journal Article
Język:
English
Imprint Name(s):
Original Publication: Philadelphia, Institute for Clinical Science.
MeSH Terms:
Abdominal Neoplasms/*pathology
Ganglioneuroblastoma/*secondary
Lymph Nodes/*pathology
Abdominal Neoplasms/surgery ; Child ; Ganglioneuroblastoma/surgery ; Humans ; Lymph Nodes/surgery ; Male ; Prognosis
Contributed Indexing:
Keywords: composite neuroblastoma; lymph node; metastatic; nodular ganglioneuroblastoma
Entry Date(s):
Date Created: 20210828 Date Completed: 20210906 Latest Revision: 20210906
Update Code:
20240105
PMID:
34452899
Czasopismo naukowe
Objective: Composite neuroblastoma is a tumor composed of multiple tumoral clones within the neuroblastoma family. To date, establishing this unique histopathologic diagnosis has required the evaluation of the primary tumor mass. We report a case of composite neuroblastoma diagnosed by evaluation of a metastatic lymph node.
Methods: One abdominal lymph node involved by tumor was evaluated in a 6-year-old boy. The primary abdominal mass was not examined. Following histopathologic examination, clonality studies using comparative genomic hybridization (CGH) and fluorescence in situ hybridization (FISH) were also performed.
Results: Two distinct tumor components were identified by histopathologic evaluation and classified as differentiating neuroblastoma (component A) and poorly differentiated neuroblastoma (component B). Based on the patient's age, each clone was further classified as Unfavorable Histology. The presence of these two different tumoral clones was confirmed by CGH and FISH.
Conclusion: This case affirms the histopathologic approach to evaluating composite tumors, as established by the International Neuroblastoma Pathology Classification (INPC) model for ganglioneuroblastoma, nodular tumors. Also, when both components are metastatic, this case demonstrates that composite tumors can be diagnosed by the evaluation of metastatic lesions alone. Finally, it supports the addition of composite neuroblastoma to a future version of the INPC.
(© 2021 by the Association of Clinical Scientists, Inc.)

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