Results 1 to 10 of about 5,290 (226)

ALK-positive histiocytosis involving the cavernous sinus: A deceptive radiologic mimic of meningioma

Radiology Case Reports, 2023
Anaplastic lymphoma kinase (ALK)-positive histiocytosis is an uncommon condition, recently considered a separate condition from other histiocytosis by WHO 5th edition. It can involve intracranial structures.
Mohammadreza Alizadeh, MD, Aishwarya Ravindran, MD, Rati Chkheidze, MD, Gaurav Goyal, MD, Mahdie Hosseini, MD, Parnian Shobeiri, MD, Arezoo Shafieioun, MD, Mohammad Khalafi, MD, Ramin Shahidi, Houman Sotoudeh, MD, Aparna Singhal, MD   +10 more
doaj   +1 more source

Patient with Rosai-Dorfman-Destombes disease: 18F-FDG-PET/CT scan as a diagnostic tool

Acta Médica Peruana, 2023
Rosai-Dorfman-Destombes disease (RDD) is a rare non-Langerhans cell histiocytosis, with sinus involvement and massive lymphadenopathy. RDD is usually self-limited; it can appear alone or related to other diseases. We present a 9-year-old male with biopsy
Luis C. Araujo Cachay
doaj   +1 more source

Sinus Histiocytosis with Massive Lymphadenopathy [PDF]

Leukemia & Lymphoma, 1992
To date, the morphological aspects of sinus histiocytosis with massive lymphadenopathy (SHML) have been fully described. The disease is characterized by an enlargement of lymph nodes in which the sinuses are dilated and infiltrated by histiocytes, often phagocytosing lymphocytes.
SACCHI, Stefano, ARTUSI, Tullio, TORELLI, Umberto, EMILIA, Giovanni   +3 more
openaire   +7 more sources

Sinus Histiocytosis with Massive Lymphadenopathy [PDF]

Indian Journal of Otolaryngology and Head and Neck Surgery, 2006
Sinus Histiocytosis with Massive Lymphadenopathy is a very rare condition often presenting as neck swelling of unknown etiology. The disease involves extranodal sites in 20-30 percent of cases and histologically characterized by emperiopolesis, non-cohesive and non-epitheloid histocytes with abundant eosinphilic cytoplasm.
Faisal Haque, Nisar Hussain Dar, Hidayatullah, S. A. Hasan, Samiullah   +4 more
openaire   +3 more sources

A case of disseminated extranodal Rosai–Dorfman disease diagnosed by skin manifestations

Journal of Cutaneous Immunology and Allergy, 2023
Rosai–Dorfman disease (RDD) is a rare non‐Langerhans cell histiocytosis that was first described as sinus histiocytosis with massive lymphadenopathy by Rosai and Dorfman in 1969.
Shintaro Saito, Akihiko Uchiyama, Yayoi Shibusawa, Sei‐ichiro Motegi   +3 more
doaj   +1 more source

Sinus Histiocytosis with Massive Lymphadenopathy [PDF]

CA: A Cancer Journal for Clinicians, 1980
A 22-month-old child presented with massive cervical adenopathy accompanied by a retropharyngeal mass that caused stridor and dysphagia. Biopsy from both sides was consistent with sinus histiocytosis with massive lymphadenopathy (SHML). SHML is an unusual benign lesion that characteristically presents with painless, massive cervical adenopathy ...
James Dearth, David Kelly, David Hunter, William Crist   +3 more
openaire   +3 more sources

Histological variability and the importance of clinicopathological correlation in cutaneous Rosai-Dorfman disease [PDF]

Anais Brasileiros de Dermatologia, 2016
: Rosai-Dorfman disease is a benign histiocytic proliferative disorder of unknown etiology. The disease mainly affects lymph node tissue, although it is rarely confined to the skin.
Ana Gameiro, Miguel Gouveia, José Carlos Cardoso, Oscar Tellechea   +3 more
doaj   +1 more source

Rosai‐Dorfman disease in 6‐year‐old child: Presentation, diagnosis, and treatment

Clinical Case Reports, 2021
Rosai‐Dorfman disease is referred to as sinus histiocytosis massive lymphadenopathy. We are reporting a rare case of Rosai‐Dorfman disease, a case of 6‐year‐old boy with a history of multiple painless submandibular and cervical lymphadenopathy.
Kalpana Giri, Ashok Baral, Niva Tiwari, Krishna Sagar Sharma   +3 more
doaj   +1 more source

Nodal histiocytic disorder in children: report of three cases and review of literature

The Egyptian Journal of Otolaryngology, 2020
Background Histiocytic system consists of phagocytes and dendritic cells. Both are found in lymph nodes. Usually, this disorder presents with painless cervical lymph node enlargement hence frequently mistaken for lymphoma or tuberculosis.
Indumathi Ainer, Hardip Singh Gendeh, Salina Binti Husain, Khadijah Mohd Nor   +3 more
doaj   +1 more source

Intriguing nodules mimicking as leprosy: An interesting case report

Clinical Dermatology Review, 2023
The differential diagnosis of disseminated infiltrated cutaneous nodules includes a plethora of disorders ranging from the more frequently encountered infective and granulomatous conditions to the obscure ones with proliferative and malignant origin ...
Vasudha A Belgaumkar, Neelam Bhatt, Ravindranath B Chavan   +2 more
doaj   +1 more source