Results 61 to 70 of about 2,665 (208)

Endoscopic treatment of mediastinal pancreatic pseudocyst using lumen apposing metal stents - Case report [PDF]

, 2023
Mediastinal pancreatic pseudocyst (PP) is a rare complication of acute alcoholic pancreatitis. Endoscopic drainage has become widely used in the management of PPs and novel lumen apposing metal stents (LAMS) could provide more effective ...
Kralj, Dominik, Kukić, Sandro, Pavić, Tajana   +2 more
core   +2 more sources

Male Parameatal Urethral Cyst: A Report of Two Cases and Literature Review

Case Reports in Urology, Volume 2026, Issue 1, 2026.
Background Parameatal urethral cysts are rare, benign cystic lesions at the urethral meatus, most often occurring in females during childhood. Fewer than 100 cases have been documented, and their pathogenesis remains unclear. This case series describes the symptoms, histological characteristics, and postoperative outcomes of two adolescent males with ...
Loukas Charalambous, Joshua Luzuriaga, Michael Ernst, Erin Bird   +3 more
wiley   +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

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

Juvenile xanthogranuloma: clinical-pathological approach. Case reports

Revista de la Facultad de Medicina Humana, 2022
Juvenile Xanthogranuloma is a non-neoplastic skin lesion of the non-Langerhans histiocytosis type, which mainly affects the pediatric population and usually has a self-limited course.
Eugenio A. Palomino Portilla, Tula D. Ayquipa Arróspide, Isaira G. Torpoco Baquerizo, María A. Medrano Huallanca, María del Pilar Quiñones Ávila   +4 more
doaj   +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

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

A neonatal pustule:Langerhans cell histiocytosis [PDF]

, 2019
Langerhans cell histiocytosis (LCH) is a rare, clinically heterogeneous disease that most commonly occurs in pediatric populations. Congenital self-limited LCH is a benign variant of LCH.
Hogeling, Marcia, Kang, Yuna, Knowles, Byron, McKenzie, Shanice, Vecerek, Natalia   +4 more
core  

Epidermal Nevi and Epidermal Naevus Syndromes

JEADV Clinical Practice, Volume 4, Issue 3, Page 669-680, August 2025.
ABSTRACT Epidermal nevi (EN) arise from postzygotic variants in ectoderm‐derived cell lines, such as keratinocytes and cells forming adnexa. EN may be present alone without any associated abnormality or be part of a syndrome. In this review, we will discuss about the clinical and genetics of the main types of EN and related syndromes.
Gianluca Tadini, Beatrice Carcano, Michela Brena   +2 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