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A second reported malignancy in a patient with Morquio syndrome
Hamza, Ameer; Khawar, Sidrah; Ibrahim, Ahmad; Edens, Jacob; Lalonde, Crystal; Danforth, Robert D.
Affiliation
  • Hamza, Ameer; St. John Hospital and Medical Center. Detroit. US
  • Khawar, Sidrah; St. John Hospital and Medical Center. Detroit. US
  • Ibrahim, Ahmad; St. John Hospital and Medical Center. Detroit. US
  • Edens, Jacob; St. John Hospital and Medical Center. Detroit. US
  • Lalonde, Crystal; UW Health Augusta Family Medicine Center. Augusta. US
  • Danforth, Robert D; St. John Hospital and Medical Center. Detroit. US
Autops. Case Rep ; 7(2): 9-14, Apr.-June 2017. ilus, tab
Article in En | LILACS | ID: biblio-905193
Responsible library: BR26.7
ABSTRACT
Morquio syndrome is a rare lysosomal storage disease that affects multiple organ systems. However, it is rarely associated with malignancy. We present the case of a 30-year old man with Morquio syndrome associated with gastric adenocarcinoma. This case also demonstrates two other findings that have not been previously described in patients with Morquio syndrome - malrotation of brainstem and cerebellum, without clinical neurologic deficit, and persistence of fetal lobulation in the kidneys.
Subject(s)
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Full text: 1 Index: LILACS Main subject: Lysosomal Storage Diseases / Mucopolysaccharidosis IV Limits: Adult / Humans / Male Language: En Journal: Autops. Case Rep Journal subject: Anatomia / Patologia Cl¡nica / Patologia Legal Year: 2017 Type: Article

Full text: 1 Index: LILACS Main subject: Lysosomal Storage Diseases / Mucopolysaccharidosis IV Limits: Adult / Humans / Male Language: En Journal: Autops. Case Rep Journal subject: Anatomia / Patologia Cl¡nica / Patologia Legal Year: 2017 Type: Article