scholarly journals Lacrimal Gland Abscess leading to Frontal Bone Chronic Osteomyelitis: A Rare Case Report

2016 ◽  
Vol 9 (2) ◽  
pp. 102-104
Author(s):  
Saurabh Varshney ◽  
Priyanka Gairola ◽  
Manu Malhotra

ABSTRACT We report a case of a 15-year-old girl presenting with left lacrimal abscess with chronic osteomyelitis of frontal bone, a rare sequelae, that of lacrimal adenitis. If lacrimal adenitis is left untreated, abscess formation can occur and can also lead to osteomyelitis. If lacrimal adenitis/abscess is diagnosed early in the disease process by understanding typical signs, conservative management can accomplish resolution without the complications and need for surgical exploration and the cosmetic implications of facial surgery. How to cite this article Varshney S, Malhotra M, Kaur N, Gairola P. Lacrimal Gland Abscess leading to Frontal Bone Chronic Osteomyelitis: A Rare Case Report. Clin Rhinol An Int J 2016;9(2):102-104.


2020 ◽  
Vol 5 (4) ◽  
pp. 287-291
Author(s):  
Ruchit Shah ◽  
◽  
Vipin Gupta ◽  
Abhishek Pandey ◽  
Danish Khan ◽  
...  


2017 ◽  
Vol 19 (1) ◽  
Author(s):  
Donya Khosravi ◽  
Maliheh Arab ◽  
Behnaz Ghavami ◽  
Maryam Shokrpour ◽  
Samaneh Sheibani ◽  
...  


2016 ◽  
Vol 4 (1) ◽  
pp. 294
Author(s):  
Krishnappa Santosh Kumar ◽  
Nanjappa Mohan Kumar

Klippel Trenaunay Syndrome (KTS) is a cutaneous vascular malformation in combination with bone and soft tissue overgrowth, with or without lymphatic malformation. Symptoms appear by birth and approximately 90% of the cases are diagnosed by the age of 12 years. Prompt diagnosis at the earliest and conservative management with regular follow up is crucial in prognosis of KTS.







2017 ◽  
Vol 4 (1) ◽  
pp. 31
Author(s):  
SushmaA Hosamani ◽  
Sunil Biradar ◽  
VG Warad


2021 ◽  
pp. 28-29
Author(s):  
Mangesh Machindra Londhe ◽  
Tushar Vithalrao Patil ◽  
Kishor H Suryawanshi ◽  
Priyanka Sunil Gaikwad

Lymphangiomas of breast are rare with only a few cases being reported so far. Among these secondary lymphangioma have been reported but cases of primary lymphangioma are even rarer. Due to its proclivity to mimic malignancy clinically, its accurate diagnosis plays a crucial role in management of these patients. This is a unique case where cytology suggested a diagnosis of vascular malformation ruling out malignancy, thus avoiding unnecessary surgical exploration along with untoward effects of chemo/radiotherapy. The histopathology revealed diagnosis of lymphangioma circumscriptum of breast



2019 ◽  
Vol 39 (7) ◽  
pp. 1030-1031 ◽  
Author(s):  
Ioannis Tsakiridis ◽  
Ioannis Chatzikalogiannis ◽  
Themistoklis Dagklis ◽  
Apostolos Athanasiadis ◽  
Apostolos Mamopoulos


2018 ◽  
Vol 32 (3) ◽  
pp. 253-256 ◽  
Author(s):  
Kauser Hina ◽  
Monga Seema ◽  
Khan Taskin ◽  
Haider Mehvish


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