A Case of a Central Conducting Lymphatic Anomaly Responsive to Sirolimus.

نویسندگان

  • Andrew McCormick
  • Stacy Rosenberg
  • Katherine Trier
  • Arcangela Balest
چکیده

The study of vascular anomalies is a rapidly progressing field in medicine. The development of new knowledge in the pathology and management of these disease processes are exemplified in the treatment of hemangiomas with propranolol and generalized lymphatic malformations with sirolimus. Central conducting lymphatic anomalies have traditionally been refractory to medical and surgical interventions. We report a case of a central conducting lymphatic anomaly that was responsive to sirolimus. A 14-year-old boy presented with chylothorax and chyluria with a lymphangiogram demonstrating abnormal lymphatic flow and reflux along the entire course of the central channels. Traditionally, medical management has been limited to somatostatin and low-fat diet with poor response and surgical interventions that are palliative. Sirolimus allows a new medical option that could improve management of this unresponsive population.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Use of Oral Sirolimus in Paediatric Patients with Serious Vascular Anomalies: Case Report

Background Pediatric vascular anomalies comprise a heterogeneous group of clinical disorders of varying severity. These anomalies are divided into vascular tumors or vascular malformations. Different therapeutic strategies have been used depending on the pathology in question. In recent years, mammalian target of rapamycin (mTOR) inhibitors have been explored as a therapeutic option in patients...

متن کامل

Treatment of the Mirror Foot with Central Ray Resection: Report of 2 Cases

The mirror foot is a rare congenital foot anomaly which is often associated with 6- to 8-toed polydactyly. Postaxial polydactyly is the most common form of this anomaly, while central polydactyly is seen infrequently. We report on 2 cases of the central mirror-foot anomaly. Calcaneus duplication and fibular hypoplasia were present in 1 case. We treated both patients by resecting the middle foot...

متن کامل

Isolated levocardia: A case report

Introduction: Levocardia with situs inversus, a rare congenital disorder, is usually associated with severe cyanotic congenital heart disease. Thus these patients have adverse prognosis. Case Report: A 2-day-old neonate with mild central cyanosis was admitted to Neonatal Intensive Care Unit (NICU). Prenatal sonographies were normal. Physical exam was normal except for 2/6 heart murmur in left s...

متن کامل

Pulmonary and pleural lymphatic endothelial cells from pediatric, but not adult, patients with Gorham-Stout disease and generalized lymphatic anomaly, show a high proliferation rate

BACKGROUND Gorham-Stout disease (OMIM 123880) and generalized lymphatic anomaly are two rare disorders of lymphendothelial growth in which thoracic involvement with chylothorax is a feared complication. Currently it is believed that both disorders are prenatal malformations that progress slowly after birth. Several pharmaceuticals with antiproliferative properties, including interferon-α-2b, ra...

متن کامل

A comparative study of fractal models and U-statistic method to identify geochemical anomalies; case study of Avanj porphyry system, Central Iran

The most significant aspect of a geochemical exploration program is to define and separate the anomalous values from the background. In the past decades, geochemical anomalies have been identified by means of various methods. Most of the conventional statistical methods aiming at defining the geochemical concentration thresholds for separating anomalies from the background have limited the effi...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Pediatrics

دوره 137 1  شماره 

صفحات  -

تاریخ انتشار 2016