Results 61 to 70 of about 6,609 (224)

Common progenitor origin for Rosai–Dorfman disease and clear cell sarcoma

The Journal of Pathology, Volume 264, Issue 3, Page 243-249, November 2024.
Abstract Histiocytic neoplasms (HNs) in adults have been reported to be associated with a high prevalence of coexisting haematological and solid malignancies. While a proportion of coexisting HNs and haematological malignancies share identical genetic alterations, the genetic association between HNs and solid malignancies has scarcely been reported. We
Aki Sato, Nozomi Yusa, Hiroyuki Takamori, Eigo Shimizu, Kazuaki Yokoyama, Satoshi Ichikawa, Hisayuki Yokoyama, Yuki Kasahara, Kodai Enda, Fumiyoshi Fujishima, Ryo Ichinohasama, Yasunori Ota, Seiya Imoto, Yasuhito Nannya   +13 more
wiley   +1 more source

Rosai-Dorfman disease presenting as stridor and hoarseness in a young female patient

Radiology Case Reports, 2023
Rosai-Dorfman disease is a non-Langherans cell histiocytosis typically revealed by lymphadenopathy. Extranodal involvement occurs in 43% and most commonly involves the head and neck, skin, and bones. Few reports have described laryngeal lesions.
Vivianne Kokje, MD, PhD, Claudio De Vito, MD, PhD, Flavia Costa Varela, MD, Yan Monnier, MD, PhD, Nicolas Dulguerov, MD, Minerva Becker, MD, Maxime Mermod, MD, PhD   +6 more
doaj  

Extranodal manifestation of Rosai-Dorfman disease in the breast tissue [PDF]

, 2016
A 71-year-old asymptomatic female with a history of breast cancer status after right total mastectomy had interval development of several new nodules in the left breast in a 1-year time span.
Ansari, Umer, Cundiff, Maria, Davis, Fiona, Keshav, Nandan, Zhou, Qiao   +4 more
core   +1 more source

Isolated unilateral eyelid Rosai–Dorfman disease

Oman Journal of Ophthalmology, 2018
Isolated eyelid Rosai–Dorfman disease without orbital disease or systemic involvement is very rare and needs a high degree of suspicion. In this report, we describe a 16-year-old boy who presented with isolated eyelid Rosai–Dorfman disease involving the ...
Nandini Bothra, Swathi Kaliki, Swarnalata Gowrishankar, S Anuradha   +3 more
doaj   +1 more source

Primary Rosai-Dorfman Disease in 39-Year-Old Woman With Osseous Tibial Lesion Manifestion: A Case Report and Literature Review

Foot & Ankle Orthopaedics, 2021
Rosai-Dorfman disease (RDD), otherwise known as sinus histiocytosis with massive lymphadenopathy (SHML), is a very rare and typically benign disorder of unknown etiology with
Jasmin Mansoori DPM, Olivia Fisher MD, MPH, Ivana O. Akinyeye DPM, Michael A. Sobolevsky DPM, Robert H. Quinn MD   +4 more
doaj   +1 more source

Erdheim–Chester disease: An elusive diagnosis in a 50‐year‐old Ethiopian man presenting with diffuse sclerotic bone lesion

Clinical Case Reports, Volume 12, Issue 9, September 2024.
Key Clinical Message Diagnosis of Erdheim–Chester disease (ECD) requires the clinician to be familiar with its various manifestations, classic radiologic and histologic features. This case highlights the significance of considering ECD in any patient presenting with bone pain and symmetric osteosclerosis of long bones of extremities to allow for early ...
Semir Abdi Usmael, Addisu Alemu Gebrehiywot, Ashenafi Lemma Bekele, Solomon Bishaw Yezengaw, Tekalign Tsegaye Tefera, Hunduma Bikila Bote, Kalkidan Abera Shibeshi, Anteneh Belachew Fantaye   +7 more
wiley   +1 more source

Disseminated histiocytoses biomarkers beyond BRAFV600E: frequent expression of PD-L1. [PDF]

, 2015
The histiocytoses are rare tumors characterized by the primary accumulation and tissue infiltration of histiocytes and dendritic cells. Identification of the activating BRAFV600E mutation in Erdheim-Chester disease (ECD) and Langerhans cell histiocytosis
Arceci, Robert J, Bender, Ryan P, Bilalovic, Nurija, Gatalica, Zoran, Millis, Sherri Z, Palazzo, Juan P., Swensen, Jeffrey, Von Hoff, Daniel, Vranic, Semir   +8 more
core   +3 more sources

Benign and malignant cutaneous nasal lesions

Eye &ENT Research, Volume 1, Issue 2, Page 65-91, September 2024.
Abstract The nose is a structure of both cosmetic and functional importance. Cutaneous lesions of the nose occasionally represent a diagnostic challenge and involve the expertise of several specialties from dermatology, otolaryngology—head and neck surgery, infectious disease, and pathology, among others.
Hamed Sarikhani, Karena Zhao, Marc A. Polacco, Charles Gropper, Samuel N. Helman   +4 more
wiley   +1 more source

Rosai-Dorfman Disease: A previously unreported association with Sickle Cell Disease [PDF]

, 2007
BACKGROUND: Rosai-Dorfman Disease is an uncommon benign systemic histio-proliferative disease. This is the first time the disease, although more common in people of African descent, is described in association with Sickle cell disease. CASE PRESENTATION:
Inusa, Baba, Ramadan, Ghada, Stebbing, Claire, van der Walt, Jon   +3 more
core   +2 more sources

Steroid responsive cavernous sinus syndrome due to Rosai-Dorfman disease: beyond Tolosa-Hunt syndrome – a case report

BMC Neurology, 2021
Background The term “Tolosa-Hunt syndrome” (THS) has been used to refer to painful ophthalmoplegia associated with nonspecific inflammation of the cavernous sinus and many processes can result in a similar clinical picture, including infectious ...
Paulo Ribeiro Nóbrega, Pedro Gustavo Barros Rodrigues, Isabelle de Sousa Pereira, Carolina de Figueiredo Santos, Gunter Gerson, José Arnaldo Motta de Arruda, José Wagner Leonel Tavares Júnior, Pablo Picasso de Araújo Coimbra, Pedro Braga-Neto   +8 more
doaj   +1 more source