Lipoblastoma with unique localization requiring tracheal and esophageal resection

Torre, Michele; Borel, Cecilia; Saitua, Francisco; Ossandon, Francisco J.; Latorre, Juan José; Varela, Patricio

doi:10.1016/j.jpedsurg.2010.06.034

Cited by 12 publications

(5 citation statements)

References 12 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…Inflammatory myofibroblastic tumor (n = 19) and granular cell tumor (n = 3) were the most frequent benign subtypes recorded in our population, but single cases of lipoblastoma, teratoma, and rhabdomyoma were also observed.…”

Section: Discussionmentioning

confidence: 85%

Pediatric airway tumors: A report from the International Network of Pediatric Airway Teams (INPAT)

et al. 2019

Self Cite

View full text Add to dashboard Cite

Objective Primary tracheobronchial tumors (PTTs) are rare heterogeneous lesions arising from any part of the tracheobronchial tree. Nonspecific symptoms may lead to delayed diagnosis that requires more aggressive surgical treatment. An analysis of cases collected by the International Network of Pediatric Airway Team was undertaken to ensure proper insight into the behavior and management of PTTs. Methods Patients <18 years of age with a histological confirmation of PTT diagnosed from 2000 to 2015 were included in this multicenter international retrospective study. Medical records, treatment modalities, and outcomes were analyzed. The patient presentation, tumor management, and clinical course were compared between malignant and benign histotypes. Clinical and surgical variables that might influence event‐free survival were considered. Results Among the 78 children identified, PTTs were more likely to be malignant than benign; bronchial carcinoid tumor (n = 31; 40%) was the most common histological subtype, followed by inflammatory myofibroblastic tumor (n = 19; 25%) and mucoepidermoid carcinoma (n = 15; 19%). Regarding symptoms at presentation, wheezing (P = 0.001) and dyspnea (P = 0.03) were more often associated with benign growth, whereas hemoptysis was more frequently associated with malignancy (P = 0.042). Factors that significantly worsened event‐free survival were age at diagnosis earlier than 112 months (P = 0.0035) and duration of symptoms lasting more than 2 months (P = 0.0029). Conclusion The results of this international study provide important information regarding the clinical presentation, diagnostic workup, and treatment of PTTs in children, casting new light on the biological behavior of PTTs to ensure appropriate treatments. Level of Evidence NA Laryngoscope, 130:E243–E251, 2020

show abstract

Section: Discussionmentioning

confidence: 85%

Pediatric airway tumors: A report from the International Network of Pediatric Airway Teams (INPAT)

et al. 2019

Self Cite

View full text Add to dashboard Cite

show abstract

“…According to the pathogenesis, a close relationship has been considered between lipoblastoma and fetal white adipose tissue. 7 …”

Section: Discussionmentioning

confidence: 99%

“…The second most common location has been reported in the neck and trunk. 7 Intrathoracic location of lipoblastoma is extremely rare. 9 Our case was a 15-month-old boy with a huge intratho-racic and mediastinal mass who presented with dyspnea.…”

Section: Discussionmentioning

confidence: 99%

Intrathoracic lipoblastoma in a 15-month-old infant

Geramizadeh¹,

Javadi

Foroutan

2011

Rare Tumors

View full text Add to dashboard Cite

Lipoblastoma is a rare tumor of infancy. It originates from the white fetal fat in soft tissue. The most common location of this rare tumor is extremity and to best of our knowledge less than 10 cases of intrathoracic and mediastinal lipoblastoma has been reported in the English literature. Herein we present our experience with a 15-month-old boy infant who presented with severe dyspnea. Imaging studies showed a mass in the thoracic cavity and mediastinum which was diagnosed as lipoblastoma after pathologic examination of the resected mass. Lipoblastoma has been considered as a tumor of soft tissue, but it should also be considered as a rare cause of intrathoracic masses of young children.

show abstract

“…应当警惕, 肿瘤生长于纵隔、颈部者, 压迫甚至侵润气管出现咳嗽、呼吸困难 [8] , 不及时处理则导致死亡, 本组1例肿物压迫气管死亡. 体查时肿物好散发, 位置深浅不一, 无压痛, 局部皮温正常, 表面光滑, 边界多欠清楚, 质地软硬不一, 常喜好发生各种腔内 [9] , 生长于体腔时肿物常较大 [2] , 甚至充满腹腔. .…”

Section: 肿物部位相关可引起腹痛、瘫痪、大小便失禁、unclassified

脂肪母细胞瘤病的临床诊治分析<bold>(</bold>附<bold>10</bold>例报告<bold>)</bold>

莫志强¹,

王焕民²,

秦红³

et al. 2018

Sci. Sin.-Vitae

View full text Add to dashboard Cite

Lipoblastoma with unique localization requiring tracheal and esophageal resection

Cited by 12 publications

References 12 publications

Pediatric airway tumors: A report from the International Network of Pediatric Airway Teams (INPAT)

Pediatric airway tumors: A report from the International Network of Pediatric Airway Teams (INPAT)

Intrathoracic lipoblastoma in a 15-month-old infant

脂肪母细胞瘤病的临床诊治分析<bold>(</bold>附<bold>10</bold>例报告<bold>)</bold>

Contact Info

Product

Resources

About

Lipoblastoma with unique localization requiring tracheal and esophageal resection

Cited by 12 publications

References 12 publications

Pediatric airway tumors: A report from the International Network of Pediatric Airway Teams (INPAT)

Pediatric airway tumors: A report from the International Network of Pediatric Airway Teams (INPAT)

Intrathoracic lipoblastoma in a 15-month-old infant

脂肪母细胞瘤病的临床诊治分析&lt;bold&gt;(&lt;/bold&gt;附&lt;bold&gt;10&lt;/bold&gt;例报告&lt;bold&gt;)&lt;/bold&gt;

Contact Info

Product

Resources

About

脂肪母细胞瘤病的临床诊治分析<bold>(</bold>附<bold>10</bold>例报告<bold>)</bold>