A Very Rare Case of a Bronchogenic Cyst Localized on the Scapular Region

2014 ◽  
Vol 36 (1) ◽  
pp. 40-42
Author(s):  
Olgun Kontas ◽  
Ali Yikilmaz
Keyword(s):  
Rare Case ◽  
Bronchogenic Cyst ◽  
Scapular Region

Abstract #110: Hemorrhagic Subdiaphragmatic Bronchogenic Cyst Mimicking an Adrenal Tumor: a Rare Case

2015 ◽  
Vol 21 ◽  
pp. 6
Author(s):  
Roy Guinto ◽  
Michele Ledoux ◽  
Alicia Williams ◽  
Anthony Mark
Keyword(s):  
Rare Case ◽  
Adrenal Tumor ◽  
Bronchogenic Cyst

scholarly journals A Solitary Ventral Scapular Osteochondroma causing Pseudo-winging of Scapula: A Case Report

2021 ◽  
Vol 11 (7) ◽  
Author(s):  
Eknath Pawar ◽  
Nihar Modi ◽  
Amit Kumar Yadav ◽  
Jayesh Mhatre ◽  
Sachin Khemkar ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Soft Tissue ◽  
Young Child ◽  
Chest Wall ◽  
Rare Case ◽  
Rare Presentation ◽  
Medial Border ◽  
Soft Tissue Masses ◽  
Scapular Region

Introduction: Winging of scapula is defined as a failure of dynamic stabilizing structures that anchor the scapula to the chest wall, leading to prominence of the medial border of scapula. It could be primary, secondary, or voluntary. Primary winging could be true winging due to neuromuscular causes or pseudo-winging due to osseous or soft-tissue masses. A scapular osteochondroma is a very rare presentation site and causes pseudo-winging leading to pushing away of the scapula away from the chest wall presenting as medial border prominence. Here, we are reporting a rare case of a scapular osteochondroma causing a pseudo-winging of the scapula. Case Report: A 2-year-old male child presented with painless, immobile, and non-fluctuant swelling over the left scapular region, insidious in onset and progressive in nature. On examination, a non-tender, immobile swelling was palpable with a painless and unrestricted range of motion at the shoulder joint. After evaluating radiographs and CT scan, the patient was diagnosed to have a ventral scapular osteochondroma leading to pseudo-winging of the scapula. Conclusion: Despite the rarity, a differential diagnosis of a scapular osteochondroma should be kept in mind while examining a young child presenting with a winged scapula. Keywords: Scapula, osteochondroma, pseudo-winging.

scholarly journals A Rare Case of Pulmonary Bronchogenic Cyst Associated with Bronchial Atresia in the Same Lobe

2003 ◽  
Vol 42 (6) ◽  
pp. 521-524 ◽  
Author(s):  
Kazuhiko SUZUKI ◽  
Masanori SHIRATORI ◽  
Hiroshi TANAKA ◽  
Takayuki ITOH ◽  
Kensuke OASHI ◽  
...  
Keyword(s):  
Rare Case ◽  
Bronchogenic Cyst ◽  
Bronchial Atresia

scholarly journals Rare Case of Servelle Martorelle Syndrome

2014 ◽  
Vol 10 (4) ◽  
pp. 91-94
Author(s):  
A Bhatnagar ◽  
M Deshpande
Keyword(s):  
Soft Tissue ◽  
Upper Limb ◽  
Rare Case ◽  
Prompt Treatment ◽  
Congenital Vascular Malformation ◽  
History Of ◽  
The Right ◽  
Scapular Region

Servelle Martorelle Syndrome is a congenital vascular malformation associated with soft tissue hypertrophy and bony hypoplasia. This rarely involves whole of an extremity, with involvement of part of limbs reported in literature. We present a case of a twelve year boy who presented to the Department of Plastic Surgery SGPGIMS in April 2011 ,with history of circumferential soft tissue hypertrophy involving whole of left upper limb, scapular region and axilla since birth. The entire left upper limb length was lesser than the right upper limb. Hence this is a very rare case of Servelle Martorelle Syndrome having extensive limb involvement at a very young age. Highlighted is the role of conservative treatment and close follow-up to understand the natural history of the diseases, with prompt treatment of complications. DOI: http://dx.doi.org/10.3126/kumj.v10i4.11011 Kathmandu Univ Med J 2012;10(4):91-94

Retroperitoneal bronchogenic cyst: a rare case showing the characteristic imaging feature of milk of calcium

2003 ◽  
Vol 28 (5) ◽  
pp. 716-720 ◽  
Author(s):  
E. Hisatomi ◽  
K. Miyajima ◽  
K. Yasumori ◽  
H. Okamura ◽  
M. Nonaka ◽  
...  
Keyword(s):  
Rare Case ◽  
Bronchogenic Cyst ◽  
Imaging Feature ◽  
Milk Of Calcium ◽  
Retroperitoneal Bronchogenic Cyst ◽  
Characteristic Imaging

scholarly journals Bronchogenic cyst—a rare case mimicking a laryngocoele

2017 ◽  
Vol 2017 (3) ◽  
Author(s):  
Mohammed Farid ◽  
Philip Michael
Keyword(s):  
Rare Case ◽  
Bronchogenic Cyst

scholarly journals CUTANEOUS BRONCHOGENIC CYST OVER STERNUM: A RARE CASE REPORT

2017 ◽  
Vol 3 (4) ◽  
pp. 203-204
Author(s):  
Smita Singh ◽  
Anamika Kashyap ◽  
Kiran Agarwal ◽  
Lalrinzuali Sailo
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Bronchogenic Cyst ◽  
Rare Case Report

scholarly journals Case Report: Prenatal and Postnatal Management for Fetal Bronchogenic Cysts During the COVID-19 Pandemic

2021 ◽  
Vol 9 ◽  
Author(s):  
Lin Cheng ◽  
Jie Duan ◽  
Mei Wang ◽  
Dan Lu ◽  
Huan Li ◽  
...  
Keyword(s):  
Genetic Counseling ◽  
Rare Case ◽  
Bronchogenic Cyst ◽  
Chromosomal Abnormalities ◽  
Ultrasound Examination ◽  
Fetal Mri ◽  
Postnatal Management ◽  
Upper Mediastinum ◽  
Bronchogenic Cysts

Background: A fetal bronchogenic cyst (BC) is a rare congenital anomaly with an incidence of 0.147–0.238‰. The coronavirus disease 2019 (COVID-19) pandemic, as a particular situation, hindered pregnant women from receiving periodic prenatal checkups.Case Description: Until 34+6 weeks of gestation, a fetal case of the intrathoracic cyst was found by ultrasound examination. Further, MRI examination confirmed the diagnosis of the congenital mediastinal cystic lesion, probably a BC. Genetic testing was not conducted due to the COVID-19 pandemic. At 38+5 weeks of gestation with maternal COVID-19 testing negative, a live girl was delivered by cesarean section. Five months later, the child underwent bronchocystectomy, and the postoperative pathological lesions confirmed a (right upper mediastinum) BC.Conclusion: Herein, we reported the prenatal and postnatal management for a rare case of the congenital BC by multidisciplinary approaches during the COVID-19 pandemic. Fetal MRI and screening for fetal chromosomal abnormalities are especially recommended. This case contributes to the awareness that the COVID-19 pandemic interferes with regular follow-up schedules during pregnancy and may interfere with timely performed additional tests; which leads to more accurate genetic counseling. A combination of multidisciplinary approaches, including radiology, infection control, genetic counseling, obstetrics, and pediatric surgery, is pivotal for managing fetal BC during the COVID-19 pandemic.

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