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Rosai-Dorfman Disease with Brain Damage in One Case at the National Hospital of Zinder

DOI: 10.4236/ojbd.2025.153010, PP. 101-108

Keywords: Rosai-Dorfman Disease, Polyadenopathy, Histiocytosis, Langerhans, Emperipolesis

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Abstract:

Introduction: Rosai-Dorfman-Destombes disease (MRDD), or non-Langerhansian histiocytosis, is characterized by the presence of multiple polyadenopathies. It is a rare myeloproliferative disorder of histiocytes with a broad spectrum of clinical manifestations and distinctive morphological features, with abnormal accumulation of histiocytes (in emperipolesis) in lymph nodes. Observation: A 16-year-old Black male, orphaned by his father and his mother, a housewife, from a sibling group of six (06) children, of which he is the eldest, with no particular pathological history, was admitted to our clinical haematology department at the Zinder/Niger National Hospital for chronic painless bilateral cervical polyadenopathy associated with persistent fever resistant to the usual analgesics. The diagnosis of lymph node tuberculosis was considered. The patient received standard anti-tuberculosis treatment with good compliance for six (06) months. The course was marked by persistent night sweats and fever, which remained at a plateau despite antipyretics. Repeated transfusions were observed. Conclusion: Rosai-Dorfman-Destombes disease (RDDD) is a histioproliferative disorder characterized by lymphadenopathy. It is a type of histiocytosis that usually appears in children as bilateral cervical lymphadenopathy. It can manifest itself in different ways, depending on the location of the lesion. It remains a major diagnostic challenge for clinicians. Cases involving the central nervous system are rare.

References

[1]  Destombes, P. (1965) Adenitis with Lipid Excess, in Children or Young Adults, Seen in the Antilles or Mali (4 Cases). Bulletin de la Société de Pathologie Exotique et de ses Filiales, 58, 1169-1175.
[2]  Elbaz Younes, I., Sokol, L. and Zhang, L. (2022) Rosai-Dorfman Disease between Proliferation and Neoplasia. Cancers, 14, Article No. 5271.
https://doi.org/10.3390/cancers14215271
[3]  Ravindran, A. and Rech, K.L. (2023) How I Diagnose Rosai-Dorfman Disease. American Journal of Clinical Pathology, 160, 1-10.
https://doi.org/10.1093/ajcp/aqad047
[4]  Mahzoni, P., Zavareh, M.H., Bagheri, M., Hani, N. and Moqtader, B. (2012) Intracranial Rosai-Dorfman Disease. Journal of Research in Medical Sciences, 17, 304-307.
[5]  Kutlubay, Z., Bairamov, O., Sevim, A., Demirkesen, C. and Mat, M.C. (2014) Rosai-Dorfman Disease: A Case Report with Nodal and Cutaneous Involvement and Review of the Literature. The American Journal of Dermatopathology, 36, 353-357.
https://doi.org/10.1097/dad.0b013e31829e5564
[6]  Zhang, X., Yin, W., Guo, Y., He, Y., Jiang, Z., Li, Y., et al. (2022) Rosai-Dorfman Disease of the Central Nervous System: A Clinical, Radiological, and Prognostic Study of 12 Cases. Frontiers in Oncology, 12, Article ID: 1013419.
[7]  Foré, R., Cohen-Aubart, F., Compagnat, M., Cussinet, L., Palat, S., Fauchais, A.L., et al. (2019) Atteinte neurologique isolée de la maladie de Rosai-Dorfman-Destombes. La Revue de Médecine Interne, 40, A124-A125.
https://doi.org/10.1016/j.revmed.2019.10.164
[8]  Fan, X., Liu, T., Zhang, Z., Sun, J., Niu, N., Mao, C., et al. (2023) Comparison of Neuroimaging Features of Histiocytic Neoplasms with Central Nervous System Involvement: A Retrospective Study of 121 Adult Patients. European Radiology, 33, 8031-8042.
https://doi.org/10.1007/s00330-023-09724-8
[9]  Vaquier, L., Abitbol, C., Emile, J., Dossier, A., Guyard, A. and Hourseau, M. (2022) Histiocytosis of Rosai-Dorfman-Destombes Extranodal of the Jawbone: Report of a Case and Review of the Literature. Annales de Pathologie, 42, 264-268.
https://doi.org/10.1016/j.annpat.2021.12.006
[10]  Gupta, K., Bagdi, N., Sunitha, P. and Ghosal, N. (2011) Isolated Intracranial Rosai-Dorfman Disease Mimicking Meningioma in a Child: A Case Report and Review of the Literature. The British Journal of Radiology, 84, e138-e141.
https://doi.org/10.1259/bjr/15772106
[11]  Nalini, A., Jitender, S., Anantaram, G. and Santosh, V. (2012) Rosai Dorfman Disease: Case with Extensive Dural Involvement and Cerebrospinal Fluid Pleocytosis. Journal of the Neurological Sciences, 314, 152-154.
https://doi.org/10.1016/j.jns.2011.10.002
[12]  Tummidi, S., Singh, H.K., Reddy, P.A., Sindhura, M., Kosaraju, N., Shankaralingappa, A., et al. (2021) ROSE in Rosai-Dorfman-Destombes (RDD) Disease: A Cytological Diagnosis. European Journal of Medical Research, 26, Article No. 34.
https://doi.org/10.1186/s40001-021-00505-x
[13]  Laudin, G.E., Lakha, A.B., Dullabh, N., Mohanlal, R., Jassat, R., Waja, M.F., et al. (2023) A Meta-Analysis of Cases of Rosai Dorfman Disease Reported on the African Continent and a Description of Two Cases from a Tertiary Academic Hospital in Johannesburg, South Africa. Pan African Medical Journal, 45, Article No. 130.
https://doi.org/10.11604/pamj.2023.45.130.40709
[14]  Almási, S., Pancsa, T., Tiszlavicz, L. and Sejben, A. (2023) Cerebral Manifestation and Diagnostic Dilemma of Rosai-Dorfman Disease. CNS Oncology, 12, CNS103.
https://doi.org/10.2217/cns-2023-0006
[15]  Foucar, E., Rosai, J. and Dorfman, R. (1990) Sinus Histiocytosis with Massive Lymphadenopathy (Rosai-Dorfman Disease): Review of the Entity. Seminars in Diagnostic Pathology, 7, 19-73.
[16]  Iancu, G., et al. (2021) Rosai-Dorfman Disease: Breast Involvement-Case Report and Literature Review. Medicina (Kaunas), 57, Article No. 1167.
https://pubmed.ncbi.nlm.nih.gov/34833385/
[17]  Ravi, S., Bajaj, D., Yadav, N., Ratre, S. and Pande, S. (2024) Intraventricular Presentation of Rosai-Dorfman Disease: A Case Report with Review of Literature. Egyptian Journal of Radiology and Nuclear Medicine, 55, Article No. 163.
https://doi.org/10.1186/s43055-024-01329-5
[18]  Ibrahim, A., Elserry, T.H., Hewedi, I., Khalil, H., Moharram, H. and Abdel-Latif, A.M. (2025) Intracranial Rosai-Dorfman Disease: A Retrospective Review of Seven Consecutive Cases. Egyptian Journal of Neurosurgery, 40, Article No. 48.
https://doi.org/10.1186/s41984-025-00363-3

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