scholarly journals Langerhans cell histiocytosis limited to the female genital tract: A review of literature with three additional cases

2017 ◽  
Vol 22 ◽  
pp. 4-8 ◽  
Author(s):  
Rebekah Wieland ◽  
Jenna Flanagan ◽  
Elise Everett ◽  
Sharon Mount
2003 ◽  
Vol 13 (3) ◽  
pp. 381-388 ◽  
Author(s):  
A. J. Montero ◽  
C. M. Diaz-Montero ◽  
A. Malpica ◽  
P. T. Ramirez ◽  
J. J. Kavanagh

2013 ◽  
Vol 2013 ◽  
pp. 1-3
Author(s):  
Sefa Kurt ◽  
Mehmet Tunc Canda ◽  
Aycan Kopuz ◽  
Dudu Solakoglu Kahraman ◽  
Abdullah Tasyurt

Langerhans cell histiocytosis (LCH) is a very rare disease of female genital tract, most commonly seen in vulva and unusual in postmenopausal period. Herein, we report the 8th case of pure vulvar LCH in a postmenopausal woman. We pay attention to the differential diagnosis in postmenopausal state, features of pathologic diagnosis, and treatment options.


Cancer ◽  
1991 ◽  
Vol 67 (6) ◽  
pp. 1650-1660 ◽  
Author(s):  
Constantine A. Axiotis ◽  
Maria J. Merino ◽  
Paul H. Duray

2020 ◽  
pp. 4256-4257
Author(s):  
S. J. Bourke

Pulmonary Langerhans’ cell histiocytosis is characterized by a reactive monoclonal proliferation of activated histiocytes in the distal bronchioles, resulting in inflammatory nodules, cyst formation, and fibrosis. Langerhans’ cells are a particular type of histiocyte derived from dendritic cells in the bone marrow. They normally migrate in the blood to the squamous epithelium of the skin, lungs, gastrointestinal, and female genital tract, where they are involved in antigen presentation to T cells. It presents with cough, breathlessness, and (sometimes) systemic symptoms. Chest radiography and CT typically show nodules which then cavitate and may rupture, causing pneumothorax. Corticosteroids and/or cytotoxic drugs are of some benefit, and lung transplantation is an option for progressive disease.


2019 ◽  
Vol 10 (1) ◽  
pp. 51
Author(s):  
Kavita Khoiwal ◽  
Amrita Gaurav ◽  
Shagun Tiwari ◽  
Jaya Chaturvedi ◽  
Ashok Singh

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