Results 71 to 80 of about 17,810 (241)

Histological Features of Delayed Foreign Body Granuloma With Epithelioid Histiocyte Aggregation and Eosinophilic Reaction due to Hyaluronic Acid Injection

Case Reports in Dentistry
Conclusion: We have reported a case of delayed foreign body granuloma with eosinophilic and histiocytic infiltration following injection of HA. It was suggested that the marked eosinophilic infiltration around macrophages was due to not only an allergic ...
Michiko Nishimura, Shinnichi Sakamoto, Miyako Hoshino, Yuji Miyazaki, Junichiro Yamamoto, Hideaki Sakashita, Kaoru Kusama, Kentaro Kikuchi   +7 more
doaj   +1 more source

Solitary Eosinophilic Granuloma in the Lumbar Spine: Case Report

International Clinical Neuroscience Journal, 2016
A case of a 3-year-old patient with osteolytic lesion in the lumbar region is presented. The clinic-radiological suspicion was infection, primary or metastatic tumor of spine.
Mohammad Ali Fazeli, Mohammad Reza Shahmohammadi, Zahra Janamiri, Reza Jalili Khoshnood, Hamed Javadian   +4 more
doaj   +1 more source

A rare case of solitary brain Langerhans cell histiocytosis with intratumoral hemorrhage in a patient affected by Turner syndrome [PDF]

, 2016
Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of cells with characteristics similar to bone marrow-derived Langerhans cells. The case of a young woman, affected by Turner syndrome and a solitary intraparenchymal LCH
Alafaci, C., Alafaci, E., GRANATA, Francesca, GRASSO, Giovanni, Morabito, Rosa, Salpietro, F.   +5 more
core   +2 more sources

Oral Angiolymphoid Hyperplasia With Eosinophilia Exhibiting Cutaneous‐Type Histopathologic Features: Clinical Regression Following Hormonal Withdrawal and a 50‐Year Review

Journal of Cutaneous Pathology, EarlyView.
Case report of a 30‐year‐old female. Asymptomatic, red‐purple hyperplastic lesion extending from teeth 21 to 25, with bleeding upon manipulation. Differential diagnosis included: inflammatory gingival hyperplasia, plasma cell gingivitis, leukemia, and Wegener's granulomatosis.
Pedro Vinícius Santos de Jesus, Louise Cristina Santos, Gilberth Tadeu Dos Santos Aciole, John Lennon Silva Cunha, Nicole Lonni, Matheus Antoni da Silva Costa, Elena Riet Correa Rivero, Rogério Gondak, Ricardo Luíz Cavalcanti de Albuquerque‐Júnior   +8 more
wiley   +1 more source

Histiocitosis de células de Langerhans en el raquis infantil [PDF]

, 2006
Introducción: la Histiocitosis de células de Langerhans incluye un amplio espectro de enfermedades de etiología desconocida, observada preponderantemente en niños.
Fernández, Claudio A., Miranda, María Gabriela, Pollono, Daniel G.   +2 more
core  

Granuloma facial: uma doença rara sob uma perspectiva dermatoscópica [PDF]

, 2013
The granuloma faciale is a rare and benign skin disease of unknown etiology, characterized by chronic leukocitoclastic vasculitis. It is characterized by skin lesions predominantly facial whose course is chronic and slowly progressive.
Estrozi, Bruna, Ianhez, Mayra, Teixeira, Danilo Augusto   +2 more
core   +3 more sources

Nodules in an Infant's Fingers

JEADV Clinical Practice, EarlyView.
Adnan Ahmad, Mariam Alshammari, Alsadat Mosbeh, Abeer Albazali, Kawthar Safar, Fatmah Al‐Sughayer   +5 more
wiley   +1 more source

Wells syndrome: clinical findings and management in a large cohort of 48 patients

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background and Objectives: Wells syndrome (WS) is a rare inflammatory skin disorder typically characterized by erythematous, edematous, and pruritic plaques. Despite its distinct histopathological features, WS remains an underdiagnosed disease due to its variable clinical presentations and overlap with other dermatological conditions.
Marco Adriano Chessa, Silvia Robuffo, Tullio Brunetti, Luca Rapparini, Bianca Maria Piraccini, Cosimo Misciali, Beatrice Raone, Iria Neri, Federica Filippi   +8 more
wiley   +1 more source

Clinicopathological pattern of cranial unifocal Langerhans cell histiocytosis: A study at medical college hospital

Indian Journal of Medical and Paediatric Oncology, 2015
Background: Eosinophilic granuloma (EG) of bone refers to a generally benign form of Langerhans cell histiocytosis localized to the bone. Patients may present with a solitary lesion (monostotic) or multiple sites of involvement (polyostotic).
Salma Bhat, Parvez Nazir, Humaira Bashir, Ruby Reshi, Sheema Sheikh, Rohi Wani   +5 more
doaj   +1 more source

Gouty Tophi of the Fingertips Induced by Repeated Microtrauma

JEADV Clinical Practice, EarlyView.
A. Gotor‐Rivera, R. F. Matilla‐Naumionek, J. L. Rodríguez‐Peralto, B. González Rodríguez   +3 more
wiley   +1 more source