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Reactive and clonal proliferations of histiocytes (macrophages/dendritic cells) represent a broad spectrum of disorders, which can affect virtually any organ of the body. The clinical spectrum ranges from benign, localized and self-limiting manifestations to severe multi-system disease. Hemophagocytic lymphohistiocytosis (HLH) is a frequently life-threatening, systemic hyperinflammatory process triggered by massive cytokine release by activated, reactive macrophages. Familial and secondary forms of HLH are discerned. Histiocytoses are clonal inflammatory myeloid disorders characterized by proliferations of mature histiocytes/macrophages and dendritic cells with recurrent kinase-activating mutations which result in constitutive activation of the ERK signaling pathway. Although traditionally subclassified according to the phenotype of the lesional cells, the clonal cells can show significant plasticity, and the occurrence of mixed histiocytoses is increasingly recognized. This is in part due to their derivation from a myeloid progenitor cell and explains the frequent association with clonal hematopoiesis or overt myeloid neoplasms in adults. At the joint Workshop of the Chinese Society of Hematopathology, the European Association for Haematopathology and the Society for Hematopathology on histiocytic/dendritic cell proliferations, neoplasms, and their mimics in Hefei, China, April 2024, in sessions 1 and 2 a total of 8 cases of HLH, 9 cases of reactive histiocytic proliferations and 40 cases of histiocytoses were submitted and reviewed by the panel. The latter included cases of LCH, indeterminate cell histiocytosis, Erdheim Chester disease, juvenile xanthogranuloma, Rosai Dorfman disease, multicentric reticulohistiocytosis, ALK-positive histiocytosis, and mixed histiocytoses. The present report summarizes important findings and open questions arising from discussing the workshop cases.
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http://dx.doi.org/10.1007/s00428-025-04096-4 | DOI Listing |
Acta Vet Scand
September 2025
Department of Animal Sciences (DCA), Federal University of the Semi-Arid Region - UFERSA, Avenida Francisco Mota, 572, Costa e Silva, Mossoró, 59625-900, RN, Brazil.
Background: Research on cancer in wild animals provides important insights into the mechanisms of carcinogenesis. Histiocytic sarcomas comprise a rare malignant macrophage-dendritic cell lineage neoplasm in wildlife. This study reports a case of histiocytic sarcoma in the small intestine of a collared peccary (Pecari tajacu), describing its clinical, anatomopathological, and immunohistochemical aspects.
View Article and Find Full Text PDFAnn Med Surg (Lond)
July 2025
Department of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Introduction And Importance: Crystal-storing histiocytosis (CSH) is a rare, non-neoplastic histiocytic proliferation that often complicates underlying lymphoproliferative or plasma cell disorders. The respiratory system is uncommonly involved in CSH. We present a local case of pulmonary CSH associated with marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT), along with eight additional cases identified from a literature review.
View Article and Find Full Text PDFCureus
July 2025
Internal Medicine, Institute for Social Security and Services for State Workers HG90, La Paz, MEX.
Histoid leprosy is an uncommon clinicopathological variant of Hansen's disease, characterized by distinct immunological, clinical, histological, and bacteriological features. It is regarded as an intensified form of multibacillary leprosy, marked by an enhanced cellular and humoral immune response. Clinically, this condition typically presents with well-defined papules and nodules on otherwise normal-appearing skin, frequently located on the face, trunk, and extremities of the body.
View Article and Find Full Text PDFInt J Surg Pathol
August 2025
Department of Pathology, Emory University Hospital, Atlanta, GA, USA.
Rosai-Dorfman disease (RDD) represents a clinicopathological entity within the spectrum of histiocytic neoplastic disorders, characterized by histiocytic proliferation with distinctive histopathological features and heterogeneous clinical presentations. We report an unusual presentation of thymic RDD in a 38-year-old female patient, with an anterior mediastinal soft tissue mass identified on computed tomography. Histologically, sections of the thymus demonstrated characteristic RDD features accompanied by a complex microenvironment containing both necrotizing and nonnecrotizing granulomatous inflammation.
View Article and Find Full Text PDFEur J Haematol
August 2025
Division of Hematology, Dalhousie University, Halifax, Nova Scotia, Canada.
Rosai-Dorfman-Destombes disease (RDD) is a rare histiocytic proliferation with protean clinical manifestations, resulting from the accumulation of activated histiocytes within nodal and extra-nodal tissues. The diagnosis can be missed, particularly when biopsies are obtained from extra-nodal sites, where histological features may be less specific than those observed in nodal specimens. Here, we examined a case series of 16 adults diagnosed with RDD from Vancouver, Canada between 2015 and 2025.
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