Results 111 to 120 of about 3,811 (247)

Cutaneous crystal storing histiocytosis: A case series with review of literature

Journal of Cutaneous Pathology, Volume 51, Issue 7, Page 506-512, July 2024.
Abstract Crystal‐storing histiocytosis (CSH) is a rare condition in which crystals accumulate in the cytoplasm of histiocytes and is usually associated with a lymphoplasmacytic neoplasm. Cutaneous CSH is extraordinarily rare and limited to case reports in the literature. We report two cases of this disease with cutaneous involvement.
Haya A. Homsi, Calvin Knapp III, Shruti Agrawal, Shweta Bhavsar, Jennifer S. Ko, Steven D. Billings, Shira Ronen   +6 more
wiley   +1 more source

Persistent Generalized Lymphadenopathy: A Diagnostic Conundrum—Case Report and Review of Literature

Indian Journal of Medical and Paediatric Oncology
Generalized lymphadenopathy is a nonspecific sign with heterogenous etiology including infective, inflammatory, and malignant causes. We present the case of a child who presented with generalized lymphadenopathy, involving the cervical, axillary ...
Mahin Mundra, Vaishnavi Sreenivasan, Nisha Swami, Kawaldeep Kaur, Bhavika Rishi, Aroonima Misra, Sumit Mehndiratta, Amitabh Singh   +7 more
doaj   +1 more source

Cell-in-Cell Phenomenon and Its Relationship With Tumor Microenvironment and Tumor Progression: A Review

Frontiers in Cell and Developmental Biology, 2019
The term cell-in-cell, morphologically, refers to the presence of one cell within another. This phenomenon can occur in tumors but also among non-tumor cells.
Xinlong Wang, Xinlong Wang, Yilong Li, Yilong Li, Jiating Li, Jiating Li, Le Li, Le Li, Hong Zhu, Hua Chen, Hua Chen, Rui Kong, Rui Kong, Gang Wang, Gang Wang, Yongwei Wang, Yongwei Wang, Jisheng Hu, Jisheng Hu, Bei Sun, Bei Sun   +20 more
doaj   +1 more source

Radiotherapeutic outcomes of Rosai–Dorfman disease with falx cerebri and superior sagittal sinus involvement: A rare case report with long‐term follow‐up

Clinical Case Reports, Volume 12, Issue 6, June 2024.
Key Clinical Message Intracranial RDD is rare medical event mimicking different diagnoses. Although the surgical resection is the best treatment option, but radiation therapy can also achieves long‐term suboptimal outcomes. Abstract An 83‐year‐old male with a history of tension‐type headaches was evaluated.
Hamid Nasrollahi, Susan Andalibi, Mansour Ansari, Maral Mokhtari, Ehsan Mohammad Hosseini, Mina Foroughi, Arman Sourani   +6 more
wiley   +1 more source

How to diagnose acid sphingomyelinase deficiency (ASMD) and Niemann–Pick disease type C from bone marrow and peripheral blood smears

HemaSphere, Volume 8, Issue 11, November 2024.
Sandrine Girard, Magali Pettazzoni, Roseline Froissart, Cécile Pagan, Thomas Boyer, Stephanie Dulucq, Valérie Gonçalves Monteiro, Nicolas Lechevalier, Marie Loosveld, Camille Lours, Caroline Mayeur‐Rousse, Mélanie Pannetier, Caroline Peillon, Maria‐Alessandra Rosenthal, Sonnthida Sep Hieng, Catherine Trichet, Lucile Baseggio, on behalf the French‐Speaking Cellular Haematology Group (GFHC)   +17 more
wiley   +1 more source

Enfermedad de Rosai-Dorfman cutánea: a propósito de un caso Cutaneous Rosai-Dorfman disease: a propos of a case

Revista Cubana de Hematología, Inmunología y Hemoterapia, 2013
Se presenta una paciente de 50 años de edad con lesión tumoral redondeada, no dolorosa en región inguinal, con crecimiento progresivo y formación de una placa eritematosa, con áreas de pigmentación e infiltración de tejidos profundos, así como aparición ...
Yaniurka Cruz-Camejo, Dailé Burgos-Aragüez, Yoana Flores-Veja, Haslen Hassiul Cáceres-Lavernia, Julio Jiménez-Galainena   +4 more
doaj  

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease): Report of a case in a Nigerian Teaching Hospital [PDF]

, 2011
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare, benign disease of unknown aetiology. This disease typically presents with massive, painless cervical lymphadenopathy but may occur in a wide variety of extranodal sites.
Adeyemo, W. L., Ajayi, O. F., Akinshipo, W., Effiom, O. A., Gbotolorun, O. M.   +4 more
core   +2 more sources

A 55‐year‐old man with a cerebral mass

Brain Pathology, Volume 34, Issue 6, November 2024.
Serena Ammendola, Giuseppe Kenneth Ricciardi, Valeria Barresi   +2 more
wiley   +1 more source

Cutaneous sinus histiocytosis of face of the non-Langerhans cell histiocytoses type (cutaneous Rosai — Dorfman disease)

Vestnik Dermatologii i Venerologii, 2019
An extremely rare case of sinus histiocytosis of the non-Langerhans cell histiocytoses type is described in 55-year-old patient with isolated localization of cutanious lesion on the right cheek without involvement of nodular structures.
E. V. Sokolovsky, G. N. Mikheev, M. G. Rybakova, E. B. Manasheva, V. A. Seredina   +4 more
doaj   +1 more source

Fine-needle aspiration cytology of Rosai-Dorfman disease of bone [PDF]

, 2008
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a rare, benign self-limiting condition of unknown etiology. Less than a quarter of cases have only extranodal involvement and a few cases of skeletal involvement of Rosai-Dorfman
Jing, Xin, McHugh, Jonathan B., Pu, Robert T.   +2 more
core   +1 more source