Results 71 to 80 of about 2,635 (192)

Nodules in an Infant's Fingers

JEADV Clinical Practice, EarlyView.
Adnan Ahmad, Mariam Alshammari, Alsadat Mosbeh, Abeer Albazali, Kawthar Safar, Fatmah Al‐Sughayer   +5 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

A 50‐year‐old man with a 12‐year history of extensive pachymeningeal thickening

Brain Pathology, EarlyView.
Alyssa M. Lee, Siddhartha Gaddamanugu, Kathyrn L. Eschbacher, Aishwarya Ravindran   +3 more
wiley   +1 more source

Benign and malignant cutaneous nasal lesions

Eye &ENT Research, Volume 1, Issue 2, Page 65-91, December 2024.
Abstract The nose is a structure of both cosmetic and functional importance. Cutaneous lesions of the nose occasionally represent a diagnostic challenge and involve the expertise of several specialties from dermatology, otolaryngology—head and neck surgery, infectious disease, and pathology, among others.
Hamed Sarikhani, Karena Zhao, Marc A. Polacco, Charles Gropper, Samuel N. Helman   +4 more
wiley   +1 more source

Istiocitoma fibroso maligno. Caso clinico [PDF]

, 2010
L’istiocitoma fibroso maligno è un sarcoma aggressivo dei tessuti molli, che compare più frequentemente nei muscoli degli arti e nella cavità addominale o nel retroperitoneo di giovani adulti.
Fabrizio, T., Morlino, A., Rossi, Maria Teresa, Scutari, Franco   +3 more
core  

Histiocyte‐rich ROS1‐rearranged inflammatory myofibroblastic tumour of the trachea: A rare neoplasm presenting with asthma‐like symptoms

Respirology Case Reports, Volume 12, Issue 12, December 2024.
A flow volume loop demonstrated classical upper airway obstruction pattern. Abstract Inflammatory myofibroblastic tumour is a rare tumour. We present an atypical case of Inflammatory myofibroblastic tumour which was trachea in location, histocyte rich and ROS1 rearranged.
Chin Tong Kwok, Jason Cheuk Ho Tsang, Mary Lam, Sandy Sze Ki Ho, Chi Sum Yuen, Yiu Cheong Yeung   +5 more
wiley   +1 more source

Japanese classification of pancreatic carcinoma by the Japan Pancreas Society: Eighth edition

Journal of Hepato-Biliary-Pancreatic Sciences, Volume 31, Issue 11, Page 755-768, November 2024.
Ishida and colleagues report that the eighth edition of the Japanese classification of pancreatic carcinoma retains the T category, introduces new lymph node names, incorporates peritoneal cytology into the M category, and addresses endoscopic ultrasound‐guided fine‐needle aspiration biopsy and post‐therapy effects.
Masaharu Ishida, Tsutomu Fujii, Masashi Kishiwada, Kazuto Shibuya, Sohei Satoi, Makoto Ueno, Kohei Nakata, Shigetsugu Takano, Katsunori Uchida, Nobuyuki Ohike, Yohei Masugi, Toru Furukawa, Kenichi Hirabayashi, Noriyoshi Fukushima, Shuang‐Qin Yi, Hiroyuki Isayama, Takao Itoi, Takao Ohtsuka, Takuji Okusaka, Dai Inoue, Hirohisa Kitagawa, Kyoichi Takaori, Masaji Tani, Yuichi Nagakawa, Hideyuki Yoshitomi, Michiaki Unno, Yoshifumi Takeyama   +26 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

Noonan syndrome‐like disorder: Case report and review of the literature

Pediatric Dermatology, Volume 41, Issue 6, Page 1203-1210, November/December 2024.
Abstract Of patients with a Noonan syndrome phenotype, only about 1% are found to be related to pathological variants in CBL, also known as Noonan syndrome‐like disorder (NSLD). We present a case of a 4‐year‐old boy diagnosed with NSLD, presenting with multiple melanocytic nevi and superficial neurofibromas.
Kristie Mar, Joseph M. Lam
wiley   +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