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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Ascites in a patient with episodic angio-oedema and eosinophilia: Thinking outside the box

Thumbnail
Συγγραφέας
Rigopoulou E.I., Ioannou M., Papadamou G., Dalekos G.N.
Ημερομηνία
2017
Γλώσσα
en
DOI
10.1136/bcr-2017-219467
Λέξη-κλειδί
complement component C1q
complement component C1q esterase inhibitor
complement component C1s inhibitor
complement component C3
complement component C4
complement inhibitor
corticosteroid
prednisolone
unclassified drug
steroid
abdominal distension
abdominal pain
abdominal ultrasound
adult
angioneurotic edema
Article
ascites
asthma
bone marrow biopsy
case report
differential diagnosis
drug dose reduction
echography
eosinophil count
eosinophilia
eye edema
face edema
female
genetic screening
Gleich syndrome
hospital readmission
human
human tissue
laboratory test
low drug dose
neck swelling
physical examination
protein blood level
weight gain
young adult
Angioedema
ascites
eosinophilia
treatment outcome
Angioedema
Ascites
Eosinophilia
Female
Humans
Steroids
Treatment Outcome
Young Adult
BMJ Publishing Group
Εμφάνιση Μεταδεδομένων
Επιτομή
Episodic angio-oedema with eosinophilia (EAE) or Gleich's syndrome is a rare condition characterised by recurrent episodes of oedema and eosinophilia, accompanied by urticaria, fever and weight gain. The presence of ascites has not been reported so far. We report a 21-year-old Caucasian woman who presented with marked ocular oedema and ascites. Laboratory evaluation revealed marked eosinophilia. During the last 3 months, three episodes of facial and neck oedema were reported, which resolved spontaneously over a period of 3-5 days. The diagnosis of EAE was established after exclusion of secondary causes (infections, allergic reactions, collagen diseases, neoplasms) and clonal disorders associated with marked eosinophilia. Low-dose steroids resulted in eosinophil decrease and complete resolution of symptoms, including ascites. This case highlights that ascites can be a very rare manifestation of EAE particularly if other more frequent causes of ascites have been excluded and the clinical and laboratory findings are supportive of EAE. © BMJ Publishing Group Ltd .
URI
http://hdl.handle.net/11615/78510
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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