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Von Hippel-Lindau (VHL) is an autosomal dominant, neoplas

Von Hippel-Lindau (VHL) is an autosomal dominant, neoplas B729X
Von Hippel-Lindau (VHL) is an autosomal dominant, neoplastic syndrome. It is caused by genetic aberration of the tumor suppressor gene VHL. It is characterized by multi-organ neoplastic lesions such as hemangioblastoma in CNS, renal cell carcinoma (RCC), and neuroendocrine tumors. By the age of 60, up to 70 % of patients develop RCC [1]. The most common sites for RCC metastasis are the lung, lymph nodes, bones, and liver. However testicular metastasis from RCC is rare and bilateral testicular metastasis is extremely rare [2, 3]. In this article, we present a VHL case with synchronous bilateral testicular metastasis from RCC.
Von
Hippel-Lindau
(VHL) is an autosomal dominant, neoplastic syndrome. It
is caused
by genetic aberration of the tumor suppressor gene VHL. It
is characterized
by multi-organ neoplastic lesions such as
hemangioblastoma
in CNS, renal cell carcinoma (RCC), and neuroendocrine tumors. By the age of 60, up to 70 % of patients develop RCC [1]. The most common sites for RCC
metastasis
are the lung, lymph nodes, bones, and liver.
However
testicular
metastasis
from RCC is rare and bilateral testicular
metastasis
is
extremely
rare [2, 3]. In this article, we present a VHL case with synchronous bilateral testicular
metastasis
from RCC.
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IELTS academic Von Hippel-Lindau (VHL) is an autosomal dominant, neoplas

Academic
  American English
1 paragraphs
100 words
This writing has been penalized,
text can't be
less than 250 words in Task 2
and less than 150 words in Task 1
5.0
Overall Band Score
Coherence and Cohesion: 5.5
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Lexical Resource: 6.0
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Task Achievement: 5.0
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