Literature DB >> 25241096

Complex lymphatic anomalies.

Cameron C Trenor1, Gulraiz Chaudry2.   

Abstract

Complex lymphatic anomalies include several diagnoses with overlapping patterns of clinical symptoms, anatomic location, imaging features, hematologic alterations, and complications. Lymphatic malformations likely arise through anomalous embryogenesis of the lymphatic system. Analysis of clinical, imaging, histologic, and hematologic features is often needed to reach a diagnosis. Aspiration of fluid collections can readily define fluid as chylous or not. The presence of chyle indicates dysfunction at the mesenteric or retroperitoneal level or above the cisterna chyli due to reflux. The imaging patterns of generalized lymphatic anomaly (GLA) and Gorham-Stout disease have been segregated with distinctive bone lesions and peri-osseous features. More aggressive histology (spindled lymphatic endothelial cells), clinical progression, hemorrhage, or moderate hematologic changes should raise suspicion for kaposiform lymphangiomatosis. Biopsy may be needed for diagnosis, though avoidance of rib biopsy is advised to prevent iatrogenic chronic pleural effusion. Lymphangiography can visualize the anatomy and function of the lymphatic system and may identify dysfunction of the thoracic duct in central conducting lymphatic anomalies. Local control and symptom relief are targeted by resection, laser therapy, and sclerotherapy. Emerging data suggest a role for medical therapies for complications of complex lymphatic anomalies. Outcomes include recurrent effusion, infection, pain, fracture, mortality, and rarely, malignancy. Complex lymphatic anomalies present significant diagnostic and therapeutic challenges. Results from a phase 2 study of sirolimus in these and other conditions are expected in 2014. Improved characterization of natural history, predictors of poor outcomes, responses to therapy, and further clinical trials are needed for complex lymphatic anomalies.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Generalized lymphatic anomaly; Gorham–Stout disease; Kaposiform lymphangiomatosis

Mesh:

Year:  2014        PMID: 25241096     DOI: 10.1053/j.sempedsurg.2014.07.006

Source DB:  PubMed          Journal:  Semin Pediatr Surg        ISSN: 1055-8586            Impact factor:   2.754


  30 in total

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2.  Pseudotumor cerebri in kaposiform lymphangiomatosis: a case report and pathogenetic hypothesis.

Authors:  Cristina Barceló-López; Antonio L López-Guerrero; Antonio García-López; José Hurtado-Marín; Helena Alarcón-Martínez; Juan F Martínez-Lage
Journal:  Childs Nerv Syst       Date:  2018-04-13       Impact factor: 1.475

Review 3.  Abdominal lymphatic malformations.

Authors:  W A Wohlgemuth; R Brill; L M Dendl; F Stangl; D Stoevesandt; A G Schreyer
Journal:  Radiologe       Date:  2018-11       Impact factor: 0.635

4.  Imaging features of kaposiform lymphangiomatosis.

Authors:  Pradeep Goyal; Ahmad I Alomari; Harry P Kozakewich; Cameron C Trenor; Antonio R Perez-Atayde; Steven J Fishman; Arin K Greene; Raja Shaikh; Gulraiz Chaudry
Journal:  Pediatr Radiol       Date:  2016-04-06

Review 5.  The Lymphatic Circulation in Adaptations to the Fontan Circulation.

Authors:  Sabarinath Menon; Murthy Chennapragada; Shinya Ugaki; Gary F Sholler; Julian Ayer; David S Winlaw
Journal:  Pediatr Cardiol       Date:  2017-02-16       Impact factor: 1.655

6.  Efficacy of systemic sirolimus in the treatment of generalized lymphatic anomaly and Gorham-Stout disease.

Authors:  Kiersten W Ricci; Adrienne M Hammill; Paula Mobberley-Schuman; Stephen C Nelson; Julie Blatt; Julia L Glade Bender; Catherine C McCuaig; Anna Synakiewicz; Ilona J Frieden; Denise M Adams
Journal:  Pediatr Blood Cancer       Date:  2019-01-22       Impact factor: 3.167

7.  Successful Treatment of a Case with Cervical Lymphatic Malformation: Repeated Bleomycin Sclerotherapy.

Authors:  Mustafa Mert Başaran; Selmin Özgürsoy Karataylı; Arzu Pampal; Şefik Halit Akmansu
Journal:  Turk Arch Otorhinolaryngol       Date:  2017-10-02

8.  Rapamycin reversal of VEGF-C-driven lymphatic anomalies in the respiratory tract.

Authors:  Peter Baluk; Li-Chin Yao; Julio C Flores; Dongwon Choi; Young-Kwon Hong; Donald M McDonald
Journal:  JCI Insight       Date:  2017-08-17

9.  Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly.

Authors:  Dong Li; Tara L Wenger; Christoph Seiler; Michael E March; Alvaro Gutierrez-Uzquiza; Charlly Kao; Elizabeth Bhoj; Lifeng Tian; Misha Rosenbach; Yichuan Liu; Nora Robinson; Mechenzie Behr; Rosetta Chiavacci; Cuiping Hou; Tiancheng Wang; Marina Bakay; Renata Pellegrino da Silva; Jonathan A Perkins; Patrick Sleiman; Michael A Levine; Patricia J Hicks; Maxim Itkin; Yoav Dori; Hakon Hakonarson
Journal:  Hum Mol Genet       Date:  2018-09-15       Impact factor: 6.150

10.  Initial Experience With Propranolol Treatment of Lymphatic Anomalies: A Case Series.

Authors:  June K Wu; Ellen D Hooper; Sherelle L Laifer-Narin; Lynn L Simpson; Jessica Kandel; Carrie J Shawber
Journal:  Pediatrics       Date:  2016-08-25       Impact factor: 7.124

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