Results 51 to 60 of about 1,567 (177)

CD68-negative nonlipidized juvenile xanthogranuloma

Dermatologica Sinica, 2017
Juvenile xanthogranuloma (JXG) belongs to the group of non-Langerhans cell histiocytosis. JXG is typically factor XIIIa- and CD68-positive. Nonlipidized JXG (NJXG) is a rare, mononuclear variant of JXG that shows few or absence of foam cells or Touton ...
Tzu-Kun Lo, Kung-Chao Chang, Chia-Bao Chu, Julia Yu-Yun Lee   +3 more
doaj   +1 more source

Exceptionally large juvenile xanthogranuloma – a case report

Liječnički vjesnik, 2023
Juvenile xanthogranuloma (JXG) is a rare, benign skin lesion pathologically classified as a non-Langerhans cell histiocytosis. The lesions appear within the first year of life in 75% of patients, predominantly on the head or neck, growing up to 5mm in ...
Luka Bulić, Eva Brenner, Suzana Ožanić Bulić   +2 more
doaj   +1 more source

Intraocular juvenile xanthogranuloma masquerading as conjunctivitis in an adult

Journal of Clinical Ophthalmology and Research, 2015
A 22-year-old female presented to us with redness, pain and intermittent blurring of vision in the left eye of one month duration. She had been diagnosed as a case of conjunctivitis elsewhere for which she was being treated with topical antibiotics ...
Ramesh Murthy, Aratee Palsule, Sujit Joshi, Madhav Bhatt   +3 more
doaj   +1 more source

Update on Pediatric Dermoscopy in Lighter Phototypes: Changes During the Evolution of the Diseases and Clues Predicting Response to Treatments

Dermatologic Therapy, Volume 2026, Issue 1, 2026.
Dermoscopy is a noninvasive tool that enables the visualization of skin lesions with magnification, allowing for more accurate diagnosis. Over the years, it has evolved from a utility in differentiation between malignant and benign neoplasms to administration in the vascular, inflammatory, and infectious dermatoses.
Vincenzo Piccolo, Giuseppe Argenziano, Andrea Bassi, Ramon Grimalt, Dirk Van Gysel, Mario Cutrone, Teresa Russo, Julia Nowowiejska-Purpurowicz, Suraiya Saleem   +8 more
wiley   +1 more source

Multiple juvenile xanthogranuloma: A rare case of having clinical appearance mimicking molluscum contagiosum or syringoma [PDF]

JDVI (Journal of General Procedural Dermatology & Venereology Indonesia), 2015
Introduction: Juvenile xanthogranuloma (JXG) is an uncommon benign cutaneous fibrohistiocytic, self healing, class II non-Langerhan’s cell histiocytosis (NLCH). JXG accounts for 80-90% of cases of NLCH.
Heru Nugraha, Siti Aisah Boediardja, Ridha Rosandi, Evelyn Lina Nainggolan, Githa Rahmayunita, Triana Agustin, Rahadi Rihatmadja   +6 more
doaj   +1 more source

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

Multiple juvenile xanthogranuloma

Dermatology Online Journal
Juvenile xanthogranuloma is the most frequent form of non-Langerhans cell histiocytosis in children. Clinically, it presents as well defined, yellowish papules that are typically located on the head, neck, upper trunk, and proximal region of the extremities.
Garcia-Sirvent, Lucia, Espineira-Sicre, Joaquin, Ruiz-Sanchez, Juan, Cuesta-Montero, Laura   +3 more
openaire   +4 more sources

Nodules in an Infant's Fingers

JEADV Clinical Practice, Volume 5, Issue 2, Page 722-724, June 2026.
Adnan Ahmad, Mariam Alshammari, Alsadat Mosbeh, Abeer Albazali, Kawthar Safar, Fatmah Al‐Sughayer   +5 more
wiley   +1 more source

The Clinicopathologic Spectrum of Rosai–Dorfman–Destombes Disease in Adults: An Analysis of 16 Cases

European Journal of Haematology, Volume 115, Issue 6, Page 555-564, December 2025.
ABSTRACT Rosai–Dorfman–Destombes disease (RDD) is a rare histiocytic proliferation with protean clinical manifestations, resulting from the accumulation of activated histiocytes within nodal and extra‐nodal tissues. The diagnosis can be missed, particularly when biopsies are obtained from extra‐nodal sites, where histological features may be less ...
Mark Trinder, Collin Pryma, Emily Leung, Graham W. Slack, Pedro Farinha, Sean Young, Neval Ozkaya, Mollie Carruthers, Luke Y. C. Chen   +8 more
wiley   +1 more source

Puzzle histiocytosis (solitary mononuclear xanthogranuloma with LCH component). A case report*

Polish Journal of Pathology, 2017
We report a case of 40-year-old Caucasian man presented with an asymptomatic nodule localized on his arm. The puzzle histiocytosis composed of juvenile xanthogranuloma and Langerhans cell histiocytosis was diagnosed.
Katarzyna Woszczyna-Mleczko, Artur Kowalik, Agnieszka Harazin-Lechowska, Piotr Bobkiewicz, Andrzej Marszałek, Janusz Ryś   +5 more
doaj   +1 more source