Literature DB >> 28080951

Primary Upper Limb Lymphedema: Case Report of a Rare Pathology.

Michael Ec Mcfarlane1.   

Abstract

INTRODUCTION: Lymphedema is characterized by a defect in the lymphatic system that causes limb swelling. Impaired uptake and transport of lymphatic fluid through lymphatic vessels causes accumulation of protein-rich fluid in the interstitial spaces, which leads to swelling of the limb. Primary lymphedema often presents at birth. The rare cases that arise after age 35 years are described as lymphedema tarda. The great majority of patients with lymphedema have swelling of the lower limbs-upper limb lymphedema is a rare disorder. CASE
PRESENTATION: An 84-year-old woman presented with a 3-year history of unilateral swelling of the right upper limb. There were no constitutional symptoms and no evidence of lymphadenopathy or systemic disease. Blood tests, carcinoembryonic antigen test, computed tomography scans, and venous Doppler ultrasound were all normal. The diagnosis was primary upper limb lymphedema. DISCUSSION: The swelling that occurs in upper limb lymphedema is permanent and usually extends to the hand. About one-third of patients with this condition also present with lower limb lymphedema. Thorough investigations are warranted in cases of unilateral upper limb lymphedema to rule out occult malignancy and systemic disease.

Entities:  

Mesh:

Year:  2016        PMID: 28080951      PMCID: PMC5224806          DOI: 10.7812/TPP/16-010

Source DB:  PubMed          Journal:  Perm J        ISSN: 1552-5767


  25 in total

1.  A new classification system for primary lymphatic dysplasias based on phenotype.

Authors:  F Connell; G Brice; S Jeffery; V Keeley; P Mortimer; S Mansour
Journal:  Clin Genet       Date:  2010-05       Impact factor: 4.438

Review 2.  Unilateral extremity swelling in female patients with cancer.

Authors:  S Samdani; E Lachmann; W Nagler
Journal:  J Womens Health Gend Based Med       Date:  2001-05

3.  Treatment of secondary lymphedema of the upper limb with CYCLO 3 FORT.

Authors:  R V Cluzan; F Alliot; S Ghabboun; M Pascot
Journal:  Lymphology       Date:  1996-03       Impact factor: 1.286

4.  [Identification of VEGFR3 gene mutation in a Chinese family with autosomal dominant primary congenital lymphoedema].

Authors:  Ji-qun Sheng; Feng Zeng; Chang Li; Jing-yu Liu; Qing Wang; Mu-gen Liu
Journal:  Zhonghua Yi Xue Yi Chuan Xue Za Zhi       Date:  2010-08

Review 5.  Lymphedema.

Authors:  S G Rockson
Journal:  Am J Med       Date:  2001-03       Impact factor: 4.965

6.  Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.

Authors:  A Irrthum; M J Karkkainen; K Devriendt; K Alitalo; M Vikkula
Journal:  Am J Hum Genet       Date:  2000-06-09       Impact factor: 11.025

7.  The inheritance of primary lymphoedema.

Authors:  R F Dale
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

Review 8.  Lymphedema: classification, diagnosis and therapy.

Authors:  A Szuba; S G Rockson
Journal:  Vasc Med       Date:  1998       Impact factor: 3.239

9.  The physical treatment of upper limb edema.

Authors:  O Leduc; A Leduc; P Bourgeois; J P Belgrado
Journal:  Cancer       Date:  1998-12-15       Impact factor: 6.860

10.  Primary upper-limb lymphoedema.

Authors:  S Vignes; M Arrault; A Yannoutsos; M Blanchard
Journal:  Br J Dermatol       Date:  2012-11-20       Impact factor: 9.302

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  1 in total

1.  Unilateral Primary Congenital Lymphedema of the Upper Limb in an 11-Month-Old Infant: A Clinical and Pharmacological Perspective.

Authors:  Girish Gulab Meshram; Neeraj Kaur; Kanwaljeet Singh Hura
Journal:  Open Access Maced J Med Sci       Date:  2018-09-18
  1 in total

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