Langerhans cell histiocytosis in childhood – Review, symptoms in the oral cavity, differential diagnosis and report of two cases

2014 ◽  
Vol 42 (2) ◽  
pp. 93-100 ◽  
Author(s):  
Vlasta Merglová ◽  
Daniel Hrušák ◽  
Ludmila Boudová ◽  
Petr Mukenšnabl ◽  
Eva Valentová ◽  
...  
2002 ◽  
Vol 44 (9) ◽  
pp. 759-763 ◽  
Author(s):  
U. Ernemann ◽  
M. Skalej ◽  
M. Hermisson ◽  
M. Platten ◽  
R. Jaffe ◽  
...  

2021 ◽  
Vol 25 (4) ◽  
pp. 27
Author(s):  
Dhanya Sasikumar ◽  
LathaMary Cherian ◽  
Pradeesh Sathyan ◽  
BinujaElsa Varghese

2013 ◽  
Vol 39 (3) ◽  
pp. 368-372 ◽  
Author(s):  
Andre Nathan Costa ◽  
Edson Marchiori ◽  
Gil Benard ◽  
Mariana Sponholz Araujo ◽  
Bruno Guedes Baldi ◽  
...  

On HRCT scans, lung cysts are characterized by rounded areas of low attenuation in the lung parenchyma and a well-defined interface with the normal adjacent lung. The most common cystic lung diseases are lymphangioleiomyomatosis, Langerhans cell histiocytosis, and lymphocytic interstitial pneumonia. In a retrospective analysis of the HRCT findings in 50 patients diagnosed with chronic paracoccidioidomycosis, we found lung cysts in 5 cases (10%), indicating that patients with paracoccidioidomycosis can present with lung cysts on HRCT scans. Therefore, paracoccidioidomycosis should be included in the differential diagnosis of cystic lung diseases.


2008 ◽  
Vol 33 (3) ◽  
pp. 516-517 ◽  
Author(s):  
René Fahrner ◽  
Beatrix Hoksch ◽  
Mathias Gugger ◽  
Ralph Alexander Schmid

2003 ◽  
Vol 7 (2) ◽  
pp. 129-132
Author(s):  
Susan E. Lenahan ◽  
Klaus F. Helm ◽  
Kenneth D. Hopper

Background: Erdheim–Chester disease is a rare non-Langerhans' cell histiocytosis. Objective: This case report is presented to familiarize clinicians with Erdheim–Chester disease and its differential diagnosis. Results and Conclusion: Erdheim–Chester disease presents with unique clinical and pathologic findings. Its xanthoma-like lesions can cause significant morbidity and mortality.


2012 ◽  
Vol 26 (6) ◽  
pp. 3407-3411
Author(s):  
Assya Krasteva ◽  
Elena Obreshkova ◽  
Hristina Michaylova ◽  
Evgeny Aleksiev ◽  
Angelina Kisselova ◽  
...  

2017 ◽  
Vol 44 (7) ◽  
pp. 659-661
Author(s):  
Tina Ho ◽  
Jennifer Oliver-Krasinski ◽  
Pierre Russo ◽  
Jesse Taylor ◽  
Jenna Streicher ◽  
...  

2002 ◽  
Vol 13 (4) ◽  
pp. 361-368 ◽  
Author(s):  
Rene Mahnel ◽  
Khing Hiong Tan ◽  
Rudolf Fahlbusch ◽  
Benedikt Volk ◽  
Dieter Lüdecke ◽  
...  

Author(s):  
Shevachut Chavananon ◽  
Pornpun Sripornsawan ◽  
Thirachit Chotsampancharoen

An 8-month-old girl presented with chronic mucous bloody diarrhea for 3 months. She was diagnosed as infective gastroenteritis and did not improve after antibiotic treatment. Three months subsequently, she was diagnosed with allergic gastroenteritis after developing generalized skin rash and was treated with amino acid-based formula but the symptoms of diarrhea deteriorated. The results of a biopsy of the gastrointestinal tract and skin lesions confirmed the diagnosis of Langerhans cell histiocytosis. Although Langerhans cell histiocytosis is uncommon with gastrointestinal tract involvement, Langerhans cell histiocytosis should be listed in the differential diagnosis for patients who present with chronic mucous bloody diarrhea that is unresponsive to multimodality treatment.


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