Results 31 to 40 of about 1,752 (171)

Tissue‐Resident Myeloid and Histiocytic Cells in Health and Disease: Novel Emerging Concepts

American Journal of Hematology, Volume 100, Issue 12, Page 2305-2319, December 2025.
ABSTRACT Although all myeloid cells are considered to derive from hematopoietic stem cells, the cells in each myeloid lineage are heterogeneous populations, and their distribution and functions vary, depending on underlying physiologic and pathologic processes, age, sex, and genetic and epigenetic signatures.
Peter Valent, Johann Wojta, Petri T. Kovanen, Olivier Hermine, Falko Fend, Karl Sotlar, Hildegard Greinix, Klaus Geissler, Karin Hartmann, Juliana Schwaab, Marco Herling, Laura Boccuni, Lukas Kazianka, Max Vincent John, Wolfgang R. Sperr, Carina Zierfuss, Alexandar Tzankov, Christian Sillaber, Milen Minkov, Gregor Hoermann, Matthew Collin, Hans‐Peter Horny, Torsten Haferlach, Maria Sibilia, Julien Haroche, Paul La Rosée, Alberto Orfao, Michel Arock   +27 more
wiley   +1 more source

Sinus histiocytosis with massive lymphadenopathy. Multiple skull involvements [PDF]

Journal of Korean Medical Science, 1998
Sinus histiocytosis with massive lymphadenopathy is a non-neoplastic self-limiting disease of the bone marrow stem cell origin. It is characterized by painless, bilateral cervical lymphadenopathy accompanied by fever, leukocytosis, elevated erythrocyte sedimentation rate and hypergammaglobulinemia. Extranodal involvement including bone is rare.
Y K, Park, Y W, Kim, W S, Choi, Y J, Lim
openaire   +2 more sources

Diagnostic challenges in Rosai-Dorfman-Destombes disease (case description and literature review) [PDF]

, 2018
The described clinical case presents 39-year-old patient with no clinically significant accompanying diseases. Since the beginning of October 2015, the patient has complained of fever, abdominal pain and generalized enlarged lymph nodes.
Gercheva, Liana, Spasova, Snejana, Varbanov, Hinko, Yuzeir, Sheniz   +3 more
core   +2 more sources

Rosai-Dorfman disease of the oral cavity [PDF]

, 2023
First described by J Rosai and R F Dorfman in 1969, Rosai-Dorfman disease (RDD) is a benign, self-limiting histiocytosis of unknown etiology. It is usually seen in the first two decades of life.
Bellalah, Ahlem, Charfeddine, Abir, Garma, Marwa, Omami, Mounir, Selmi, Jamil, Sioud, Sameh   +5 more
core   +2 more sources

Combination of Photodynamic and Bronchoscopic Intervention With Radiation Therapy in Treating Pulmonary Pleomorphic Sarcoma: A Case Report

The Clinical Respiratory Journal, Volume 19, Issue 9, September 2025.
We discuss a case where an innovative combination of photodynamic therapy (PDT) and local radiation therapy to address the diagnostic and therapeutic challenges associated with PPSS resulted in significant improvements in clinical symptoms and patient survival, demonstrating the success of this treatment.
Ran An, Shishou Wang, Lijian Tang, Tao Feng, Chen Lin, Chongqing Lv   +5 more
wiley   +1 more source

Sinus histiocytosis with massive lymphadenopathy. Fifteen new casesd [PDF]

Cancer, 1976
Fifteen cases of chronic lymphadenitis with massive hemophagocytic sinus histiocytosis were analyzed. Fourteen patients were whites, 13 were Europeans, and 11 were males; 10 patients were under 10, 4 were over 20, and 2 over 60 years old. The oldest patient died; all other either healed without therapy or are in excellent condition.
F, Lampert, K, Lennert
openaire   +2 more sources

Immunoglobulin G4–Related Disease of the Sternoclavicular Joint: A Case Report

Clinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT This case highlights the possibility that Immunoglobulin G4‐related disease (IgG4‐RD) lesions can also occur in the sternoclavicular joint. If a neoplastic lesion is found in the sternoclavicular joint, a biopsy should be attempted to diagnose IgG4‐RD as a differential.
Remi Mizuta, Shinnosuke Takemoto, Mutsumi Ozasa, Sawana Ono, Takahito Fukuda, Ryuta Tagawa, Fumiko Hayashi, Kazumasa Akagi, Hiromi Tomono, Hirokazu Taniguchi, Midori Matsuo, Hiroshi Gyotoku, Takahiro Takazono, Hiroshi Ishimoto, Noriho Sakamoto, Keitaro Matsumoto, Yasushi Obase, Tomoya Nishino, Hiroshi Mukae   +18 more
wiley   +1 more source

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) — imaging manifestations of renal involvement [PDF]

, 2014
A 23-year-old lady presented with abdominal fullness and distension as well as large abdominal masses in physical exam. Upon ultrasonographic evaluation, two large space occupying lesions anterior to kidneys, with no clear distinction from renal tissue ...
Gholamrezanezhad, Ali, Izadyar, Sina, Samiei, Farhad   +2 more
core   +2 more sources

Bagaimana Prognosis Histiocytosis? Sebuah Laporan Kasus [PDF]

, 2013
Penderita histiocytosis dengan keterlibatan multiorgan dan disertai gangguan fungsi organ mempunyai prognosis buruk dan tingkat mortalitas tinggi. Dilaporkan seorang penderita histiocytosis, usia 1 tahun 1 bulan yang datang dengan kelainan di kulit ...
Lestari, R. D. (Rini), Mulatsih, S. (Sri)   +1 more
core  

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