Results 31 to 40 of about 4,922,335 (121)

A Rare Case of Cutaneous Crystal‐Storing Histiocytosis With Kappa Light Chain Restriction and Unusual BCL6 Expression

Journal of Cutaneous Pathology, Volume 53, Issue 8, Page 682-686, August 2026.
ABSTRACT Crystal‐storing histiocytosis (CSH) is a rare histopathologic phenomenon characterized by the accumulation of crystalline material within histiocytes, most often associated with lymphoplasmacytic or plasma cell neoplasms. Cutaneous involvement is uncommon and may present diagnostic challenges.
Liangli Wang, Jonathan L. Curry, Julia Dai, Daniel H. Wang, Paolo Strati, Melody R. Becnel, Leomar Y. Ballester, Carlos A. Torres‐Cabala, Phyu P. Aung   +8 more
wiley   +1 more source

A Case of Indeterminate Cell Histiocytosis in an Infant [PDF]

, 2007
Indeterminate cell histiocytosis is a rare disease of predominant cells having features that resemble both Langerhans cells and macrophages. The cells have greater pleomorphism with polyobated nuclei and these cells express markers for macrophages and ...
유철주
core  

Utilizing Computer-assisted Planning for Split Calvarial Bone Cranioplasty of an Infant With Occipital Langerhans Cell Histiocytosis

Plastic and Reconstructive Surgery, Global Open
Summary:. Langerhans cell histiocytosis is frequently characterized by lytic calvarial lesions, periodically necessitating cranioplasty in infant patients.
Jordan R. Whittles, BS, William Cobb, MD, Chenue Abongwa, MD, Mohga Ali, MD, Keyne Johnson, MD, FAANS, Joseph Lopez, MD, MBA, FAAP, FACS   +5 more
doaj   +1 more source

Light Chain Crystalline Proximal Tubulopathy and Podocytopathy With Staining for Both Light and Heavy Chain Immunoglobulin

Nephrology, Volume 31, Issue 8, August 2026.
ABSTRACT A 69‐year‐old male patient presented with weight loss and proteinuria. His medical history included papillary thyroid carcinoma. Laboratory findings showed proteinuria and high κ light chain levels in both urine and serum. Bone marrow aspiration revealed plasma cell myeloma of the IgA‐κ type.
Seoyoung Choi, Kyung Chul Moon
wiley   +1 more source

Cutaneous Crystal‐Storing Histiocytosis With Marginal Zone Lymphoma. A Case Report With A Striking Clinical Presentation

Journal of Cutaneous Pathology, Volume 53, Issue 7, Page 576-580, July 2026.
ABSTRACT Cutaneous crystal‐storing histiocytosis (CSH) is an extremely rare histopathologic finding of histiocytes accumulating crystals of immunoglobulin or paraproteins, often associated with lymphoplasmacytic malignancies. It commonly presents in a wide age range of both female and male adults with a history of a lymphoproliferative disorder ...
Ashton Arlen, Brad S. Graham, Gregory A. Hosler, Marsha C. Kinney   +3 more
wiley   +1 more source

Indeterminate Cell Histiocytosis – Case Report and Review of Literature [PDF]

Serbian Journal of Dermatology and Venereology, 2018
Abstract Introduction. Indeterminate cell histiocytosis is a rare proliferative disorder of indeterminate dendritic cells, reported in only 50 case reports so far. It is clinically presented as yellow, red or brown papules and nodules that appear in otherwise healthy adult individuals.
Aleksandra R. Vojvodić, Željko Mijušković, Lidija Kandolf Sekulović   +2 more
openaire   +1 more source

A Case of Indeterminate Cell Histiocytosis [PDF]

, 2008
Indeterminate cell histiocytosis (ICH) is a rare proliferative disorder of indeterminate cells, which express S-100 and CD68 antigens and show variable reactivity for CD1a, but lack Birbeck granules.
이승헌, 김현정, 홍순원
core  

A Review of Bioarcheological Investigations in Iron Age Cambodia

International Journal of Osteoarchaeology, Volume 36, Issue 3, Page 454-468, May/June 2026.
ABSTRACT Archeological research within Cambodia is quite extensive, with significant projects led by both Cambodian archeologists and international researchers alike. Many of these projects have uncovered human skeletal remains. This article reviews archeological human skeletal studies in Cambodia, synthesizing published and unpublished data, primarily
Sophorn Nhoem, Kate Domett, Nigel Chang, Louise Shewan   +3 more
wiley   +1 more source

Isolated Adult Langerhans' Cell Histiocytosis in Cervical Lymph Nodes: Should It Be Treated?

, 2011
Objective: We report an extremely rare case of Langerhans' cell histiocytosis involving isolated cervical lymph nodes, and we discuss the diagnosis and treatment of this infrequent disease.
羅武嘉;鄭博文, Lo, W-C; Chen, C-C; Tsai, C-C; Cheng, P-W   +1 more
core   +1 more source

Spontaneous resolution of unifocal Langerhans cell histiocytosis of the skull : potential role of ultrasound in detection and imaging follow-up [PDF]

, 2018
Langerhans cell histiocytosis is a tumor-like condition characterized by idiopathic proliferation of Langerhans cells. The disease may involve the skeleton as well as other organs systems. Bone involvement may be solitary or multifocal.
Verlooy, Joris, Mania De Praeter, Filip M. Vanhoenacker, Vanhoenacker, Filip, Joris Verlooy, Vanhoenacker, Filip M., De Praeter, Mania   +6 more
core   +1 more source