Skip to main content Accessibility help

We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.

Close cookie message
×
Hostname: page-component-586b7cd67f-rcrh6 Total loading time: 0 Render date: 2024-11-26T11:35:37.335Z Has data issue: false hasContentIssue false

Section V - Histiocytic Neoplasm and Miscellaneous Bone Marrow Diseases

Published online by Cambridge University Press:  25 November 2023

Edited by
Silvia Tse Bunting ,
Xiayuan Liang ,
Michele E. Paessler  and
Satheesh Chonat
Silvia Tse Bunting
Affiliation:
Cleveland Clinic Florida Weston
Xiayuan Liang
Affiliation:
University of Colorado
Michele E. Paessler
Affiliation:
University of Pennsylvania School of Medicine
Satheesh Chonat
Affiliation:
Emory University, Atlanta
Get access
Type
Chapter
Information
Atlas of Pediatric Hematopathology , pp. 257 - 290
Publisher: Cambridge University Press
Print publication year: 2023

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

References

Rollins, BJ. Biology and genomics of LCH and related disorders. In Abla, O and Janka, G, eds. Histiocytic disorders. New York, Springer; 2018:53–71.CrossRefGoogle Scholar
Emile, JF, Abla, O, Fraitag, S, Horne, A, Haroche, J, Donadieu, J, et al. Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages. Blood. 2016; 127(22): 2672–81.CrossRefGoogle ScholarPubMed
Foucar, E, Rosai, J, Dorfman, R. Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): Review of the entity. Semin Diagn Pathol. 1990; 7(1): 19–73.Google ScholarPubMed
Henter, JI, Horne, A, Aricó, M, Egeler, RM, Filipovich, AH, Imashuku, S, et al. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer. 2007; 48(2): 124–31.CrossRefGoogle ScholarPubMed

References

Porwit, A, McCullough, J, Erber, WN. Blood and bone marrow pathology. 2nd ed. Edinburgh: Churchill Livingstone/Elsevier; 2011.Google Scholar
Proytcheva, MA. Diagnostic pediatric hematopathology. Cambridge: Cambridge University Press; 2011.CrossRefGoogle Scholar
Renella, R, Wood, WG. The congenital dyserythropoietic anemias. Hematol Oncol Clin North Am. 2009; 23: 283–306.CrossRefGoogle ScholarPubMed
Wickramasinghe, SN, Wood, WG. Advances in the understanding of the congenital dyserythropoietic anemias. Br J Haematol. 2005; 131: 431–6.CrossRefGoogle Scholar
de-la-Iglesia-Iñigo, S, Moreno-Carralero, MI, Lemes-Castellano, A, et al. A case of congenital dyserythropoietic anemia type IV. Clin Case Rep. 2017; 5: 248–52.CrossRefGoogle ScholarPubMed
Bain, BJ, Clark, DM, Wilkins, B. Bone marrow pathology. 4th ed. Chichester: Wiley-Blackwell; 2010.Google Scholar
Obut, F, Kasinath, V, Abdi, R. Post-bone marrow transplant thrombotic microangiopathy. Bone Marrow Transplant. 2016; 51: 891–7.CrossRefGoogle ScholarPubMed
Boutin, RD, White, LM, Laor, T, et al. MRI findings of serous atrophy of bone marrow and associated complications. Eur Radiol 2015; 25: 2771–8.CrossRefGoogle ScholarPubMed
Foucar, K, Reichard, K, Czuchlewski, D. Bone marrow pathology. 3rd ed. Chicago: ASCP Press; 2010.Google Scholar
Wool, GD, Deucher, A. Bone marrow necrosis: Ten-year retrospective review of bone marrow biopsy specimens. Am J Clin Pathol. 2015; 143: 201–13.CrossRefGoogle ScholarPubMed
Busuttil, DP, Liu Yin, JA. The bone marrow in hereditary cystinosis. Br J Haematol. 2000; 111: 385.Google ScholarPubMed
Foucar, K, Viswanatha, DS, Wilson, CS. Non-neoplastic disorders in bone marrow. Washington, DC: American Registry of Pathology in collaboration with the Armed Forces Institute of Pathology; 2008.CrossRefGoogle Scholar
Orchard, PJ, Fasth, AL, Le Rademacher, J, et al. Hematopoietic stem cell transplantation for infantile osteopetrosis. Blood. 2015; 126: 270–6.CrossRefGoogle ScholarPubMed
Burchill, SA, Beiske, K, Shimada, H, et al. Recommendations for the standardization of bone marrow disease assessment and reporting in children with neuroblastoma on behalf of the International Neuroblastoma Response Criteria Bone Marrow Working Group. Cancer. 2017; 123: 1095–1105.CrossRefGoogle Scholar
Kume, A, Morikawa, T, Ogawa, M, et al. Congenital neuroblastoma with placental involvement. Int J Clin Exp Pathol. 2014; 7: 8198–204.Google ScholarPubMed
Hung, YP, Lee, JP, Bellizzi, AM, et al. PHOX2B reliably distinguishes neuroblastoma among small round blue cell tumours. Histopathology. 2017; 71: 786–94.CrossRefGoogle ScholarPubMed
Maryanovich, M, Takeishi, S, Frenette, PS. Neural regulation of bone and bone marrow. Cold Spring Harb Perspect Med. 2018; 8: a031344.CrossRefGoogle ScholarPubMed
WHO Classification of Tumours Editorial Board. Soft tissue and bone tumours. 5th ed. Lyon: IARC Press; 2020.Google Scholar
Husain, AN, Stocker, JT, Dehner, LP. Stocker & Dehner’s pediatric pathology. 4th ed. Philadelphia, PA: Wolters Kluwer; 2016.Google Scholar
Smith, LM, Anderson, JR, Coffin, CM. Cytodifferentiation and clinical outcome after chemotherapy and radiation therapy for rhabdomyosarcoma (RMS). Med Pediatr Oncol. 2002; 38: 398–404.CrossRefGoogle ScholarPubMed
Hung, YP, Fletcher, CD, Hornick, JL. Evaluation of NKX2-2 expression in round cell sarcomas and other tumors with EWSR1 rearrangement: Imperfect specificity for Ewing sarcoma. Mod Pathol. 2016; 29: 370–80.CrossRefGoogle ScholarPubMed
Goldblum, JR, Folpe, AL, Weiss, SW. Enzinger and Weiss’s soft tissue tumors. 6th ed. Philadelphia, PA: Elsevier Saunders: 2014.Google Scholar
Sampson, VB, David, JM, Puig, I, et al. Wilms’ tumor protein induces an epithelial-mesenchymal hybrid differentiation state in clear cell renal cell carcinoma. PLoS One. 2014; 9: e102041.CrossRefGoogle Scholar
Zacharoulis, S, Abramson, DH, Dunkel, IJ. More aggressive bone marrow screening in retinoblastoma patients is not indicated: The Memorial Sloan-Kettering Cancer Center experience. Pediatr Blood Cancer. 2006; 46: 56–61.CrossRefGoogle Scholar
Ireland, RM. Morphology of Wolman cholesteryl ester storage disease. Blood. 2017; 126: 803.CrossRefGoogle Scholar
Miller, KP, Venkataraman, G, Gocke, CD, et al. Bone marrow findings in patients with acute promyelocytic leukemia treated with arsenic trioxide. Am J Clin Pathol. 2019; 152: 675–85.CrossRefGoogle ScholarPubMed
Burtis, CA, Ashwood, ER, Bruns, DE. Tietz textbook of clinical chemistry and molecular diagnostics. 5th ed. Philadelphia, PA: Elsevier Saunders; 2012.Google Scholar
Gregg, XT, Reddy, V, Prchal, JT. Copper deficiency masquerading as myelodysplastic syndrome. Blood. 2002; 100: 1493–5.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×