The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages
Open accessAbstract
The histiocytoses are rare disorders characterized by the accumulation of macrophage, dendritic cell, or monocyte-derived cells in various tissues and organs of children and adults. More than 100 different subtypes have been described, with a wide range of clinical manifestations, presentations, and histologies. Since the first classification in 1987, a number of new findings regarding the cellular origins, molecular pathology, and clinical features of histiocytic disorders have been identified. We propose herein a revision of the classification of histiocytoses based on histology, phenotype, molecular alterations, and clinical and imaging characteristics. This revised classification system consists of 5 groups of diseases: (1) Langerhans-related, (2) cutaneous and mucocutaneous, and (3) malignant histiocytoses as well as (4) Rosai-Dorfman disease and (5) hemophagocytic lymphohistiocytosis and macrophage activation syndrome. Herein, we provide guidelines and recommendations for diagnoses of these disorders.
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Cites
Mutations of the BRAF gene in human cancer
Davies, H., Bignell, G. R., Cox, C., Stephens, P., Edkins, S., Clegg, S., Teague, J., Woffendin, H., Garnett, M. J., Bottomley, W., et al. (2002) · Nature · doi:10.1038/nature00766 · Cited by 10,674
Vemurafenib in Multiple Nonmelanoma Cancers with BRAF V600 Mutations
Hyman, D. M., Puzanov, I., Subbiah, V., Faris, J. E., Chau, I., Blay, J.-Y., Wolf, J., Raje, N. S., Diamond, E. L., Hollebecque, A., et al. (2015) · New England Journal of Medicine · doi:10.1056/nejmoa1502309 · Cited by 1,764 · cited 5×
“Rare mutations in other MAPK pathway members including ARAF and MAP3K1 have also been reported.39,40 Finally,mutations affectingother signalingpathway such as PIK3CA, PICK1, and PICK3R2 have also been described in LCH.37,41 The presence of BRAF mutations has been investigated in nonLCHs.”
BackgroundInfluentialSelf-citationHypercytokinemia in familial hemophagocytic lymphohistiocytosis
Henter, J., Elinder, G., Soder, O., Hansson, M., Andersson, B., & Andersson, U. (1991) · Blood · doi:10.1182/blood.v78.11.2918.2918 · Cited by 505
Self-citationHypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH
Zhang, K., Jordan, M. B., Marsh, R. A., Johnson, J. A., Kissell, D., Meller, J., Villanueva, J., Risma, K. A., Wei, Q., Klein, P. S., et al. (2011) · Blood · doi:10.1182/blood-2011-07-370148 · Cited by 428
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Cited by
Khoury, J. D., Solary, E., Abla, O., Akkari, Y., Alaggio, R., Apperley, J. F., Bejar, R., Berti, E., Busque, L., Chan, J. K. C., et al. (2022) · Leukemia · doi:10.1038/s41375-022-01613-1 · Cited by 4,274
Self-citationBergsten, E., Horne, A., Aricó, M., Astigarraga, I., Egeler, R. M., Filipovich, A. H., Ishii, E., Janka, G., Ladisch, S., Lehmberg, K., et al. (2017) · Blood · doi:10.1182/blood-2017-06-788349 · Cited by 677
Self-citationRodriguez-Galindo, C., & Allen, C. E. (2020) · Blood · doi:10.1182/blood.2019000934 · Cited by 361
Self-citationMutually exclusive recurrent KRAS and MAP2K1 mutations in Rosai–Dorfman disease
Garces, S., Medeiros, L. J., Patel, K. P., Li, S., Pina-Oviedo, S., Li, J., Garces, J. C., Khoury, J. D., & Yin, C. C. (2017) · Modern Pathology · doi:10.1038/modpathol.2017.55 · Cited by 299
Goyal, G., Tazi, A., Go, R. S., Rech, K. L., Picarsic, J. L., Vassallo, R., Young, J. R., Cox, C. W., Van Laar, J., Hermiston, M. L., et al. (2022) · Blood · doi:10.1182/blood.2021014343 · Cited by 283
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Metadata
- Authors
- Emile, J.-F., Abla, O., Fraitag, S., Horne, A., Haroche, J., Donadieu, J., Requena-Caballero, L., Jordan, M. B., Abdel-Wahab, O., Allen, C. E., Charlotte, F., Diamond, E. L., Egeler, R. M., Fischer, A., Herrera, J. G., Henter, J.-I., Janku, F., Merad, M., Picarsic, J., Rodriguez-Galindo, C., Rollins, B. J., Tazi, A., Vassallo, R., & Weiss, L. M.
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2016-06-02
- Volume
- 127
- Issue
- 22
- Pages
- 2672-2681
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W2295097092
- Cited by
- 1,591
- References
- 4
- FWCI
- 86.70
- Type
- journal article
- Language
- en
- Open access
- bronze
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- The paper
- Emile, J.-F., Abla, O., Fraitag, S., Horne, A., Haroche, J., Donadieu, J., Requena-Caballero, L., Jordan, M. B., Abdel-Wahab, O., Allen, C. E., Charlotte, F., Diamond, E. L., Egeler, R. M., Fischer, A., Herrera, J. G., Henter, J.-I., Janku, F., Merad, M., Picarsic, J., . . . Weiss, L. M. (2016). Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages. Blood. https://doi.org/10.1182/blood-2016-01-690636
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