Results 41 to 50 of about 74,348 (167)
Cardiac Juvenile Xanthogranuloma in an Infant Presenting with Pericardial Effusion [PDF]
, 2012 Juvenile xanthogranuloma is a rare histiocytic disorder of childhood mainly affecting skin and rarely deep soft tissues and viscera. We report a 2‐month‐old infant who presented with respiratory distress secondary to a large pericardial effusion ...
Aggarwal, Sanjeev +3 more
core +1 more source
Eruptive papules on axillary folds of an adolescent
, 2023 Pediatric Dermatology, Volume 40, Issue 4, Page 727-729, July/August 2023.
Luca Di Bartolomeo +4 more
wiley +1 more source
Lucio phenomenon in pregnancy: A histopathology review [PDF]
, 2023 Background: Lucio phenomenon (LP) is a reaction occurring in lepromatous, non-nodular, diffuse leprosypatients who have not received multidrug therapy (MDT).
Fiqnasyani, Siti Efrida +4 more
core +2 more sources
Rare Presentation of a Rare Orthopedic Pathology: Erdheim Chester Disease [PDF]
, 2017 In 1930, William Chester and pathologist Jakob Erdheim discovered the pathology currently known as Erdheim Chester disease. There are only approximately 249 histologically confirmed patients to have been diagnosed with this disease as noted in the ...
Samona J, Owen J, Martin S
core +1 more source
Progressive nodular histiocytosis: an unusual disorder.
Dermatology Online Journal, 2021 Progressive nodular histiocytosis (PNH) is a rare type of non-Langerhans cell histiocytosis of the xanthogranuloma group. Less than 20 cases have been reported.
M. Roldán +3 more
semanticscholar +1 more source
Multicentric Reticulohistiocytosis - A Rare Clinicopathological Entity
Journal of Evolution of Medical and Dental Sciences, 2021 This is a rare case report of a thirty-eight-year-old male who presented with multiple asymptomatic hyper-pigmented papulonodular lesions on the face for the past two years without the association of pain or pruritus and with restriction of elbow ...
B. M. S., N. G.
semanticscholar +1 more source
Neonatal Systemic Juvenile Xanthogranuloma with an Ominous Presentation and Successful Treatment [PDF]
, 2011 This case report originated from a case of neonatal multisystemic juvenile xanthogranuloma (JXG). The patient presented with blue muffin rush, cervical mass, bone destruction, lung nodule, hepatosplenomegaly, and coagulopathy and was successfully treated
Fan, Rong, Sun, Jihong
core +2 more sources
Xanthogranulomatous endometritis [PDF]
, 1989 Xanthogranulomatous inflammatory changes of the endometrium are rare and appear to be related to obstructive changes in the endocervical canal. An elderly patient with an advanced squamous carcinoma of the cervix uteri presented with this condition ...
Busuttil, Anthony, Soria, M.
core
Pigmented clear cell sarcoma of soft tissue: an important diagnostic mimic [PDF]
, 2022 Clear cell sarcoma of soft tissue (CCSST) is a rare and aggressive soft tissue tumour associated with tendons and aponeuroses of the lower extremities.
De Noon, Solange +2 more
core
The American journal of case reports, 2021 Patient: Male, 63-year-old Final Diagnosis: Erdheim-Chester disease Symptoms: Splenic rupture Medication: — Clinical Procedure: Splenectomy Specialty: Anatomy • Hematology • Pathology Objective: Rare disease Background: Erdheim-Chester disease (ECD) is a
G. Di Stefano +5 more
semanticscholar +1 more source