Results 81 to 90 of about 316,660 (233)

Role of fine needle aspiration cytology in the diagnosis of juvenile xanthogranuloma in adult: Case report and review of the literature

IP Archives of Cytology and Histopathology Research, 2021
Juvenile xanthogranuloma(JXG) is an uncommon benign histiocytic cutaneous lesion which is seen primarily in first two decades of life. There is not much literature available on its cytology.
Neelam, S. Singh, R. Raina
semanticscholar   +1 more source

Pilomatricoma in the infraorbital region

Clinical Case Reports, Volume 12, Issue 8, August 2024.
Key Clinical Message Pilomatricoma, a rare benign skin tumor arising from hair follicle matrix cells, warrants consideration in the evaluation of subcutaneous nodules or masses, especially when presenting as painless and firm lesions. Accurate diagnosis hinges on histopathological examination, underscoring the significance of clinician vigilance and ...
Dilasha Dhungel, Varun Rastogi, Sandhya Chaurasia, Nisha Maddheshiya   +3 more
wiley   +1 more source

Erdheim-Chester Disease: a comprehensive review of the literature [PDF]

, 2013
Erdheim-Chester Disease (ECD) is a rare form of non Langerhans' cell histiocytosis. Individuals affected by this disease are typically adults between their 5th and 7th decades of life. Males and females are almost equally affected.
Mirra Manevich-Mazor, Roei D Mazor, Yehuda Shoenfeld   +2 more
core   +1 more source

Cysts and tumours of the iris: Diagnostic tools and key management considerations—A review

Clinical &Experimental Ophthalmology, Volume 52, Issue 6, Page 665-683, August 2024.
Abstract The iris is a unique structure, with exquisite variations in colour and form. Pathological changes, specifically including iris cysts and tumours are relatively uncommon, difficult to diagnose, and yet potentially blinding or life‐threatening.
Bia Z. Kim, Joevy Z. Lim, Charles N. J. McGhee   +2 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

Brain imaging in children with neonatal cholestatic liver disease: A systematic review

Acta Paediatrica, Volume 113, Issue 6, Page 1168-1185, June 2024.
Abstract Aim To determine if children with neonatal cholestatic liver disease had concurrent and later findings on brain imaging studies that could be attributed and the cholestasis to contribute to the understanding of the impaired neuropsychological development.
Thora Wesenberg Helt, Lars Søndergaard Johansen, Daniel Faurholt‐Jepsen, Vibeke Andrée Larsen, Lise Borgwardt, Jann Mortensen, Vibeke Brix Christensen   +6 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

Yellow and orange in cutaneous lesions: clinical and dermoscopic data [PDF]

, 2015
Colour of the lesions is clue for the clinical and dermoscopic diagnosis. Nevertheless, we have detected in the literature an uneven relevance of the colours as a diagnostic criterion.
Arribas, P., Bañuls, José, Berbegal, L., DeLeón, F.J., Francés, L., Zaballos, P.   +5 more
core   +1 more source

Demographics and additional haematologic cancers of patients with histiocytic/dendritic cell neoplasms

Histopathology, Volume 84, Issue 5, Page 837-846, April 2024.
From 1993 to 2022, more than 4000 patients with a pathologist‐assigned diagnosis of a histiocytic disorder were registered in the Dutch Nationwide Pathology Databank. This unique dataset provides an unbiased look into the demographic characteristics and additional haematologic cancers of patients diagnosed with histiocytic disorders in The Netherlands.
Paul G Kemps, Lennart Kester, Marijn A Scheijde‐Vermeulen, Carel J M van Noesel, Robert M Verdijk, Arjan Diepstra, Ariënne M W van Marion, Natasja Dors, Cor van den Bos, Annette H Bruggink, Pancras C W Hogendoorn, Astrid G S van Halteren   +11 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