Eosinophilic Ascites: A Rare Diagnosis With an Even Rarer Etiology

被引:0
|
作者
Surapaneni, Devipriya [1 ]
Azam, Bilal [2 ]
Dasi, Sharath Chandra [1 ]
机构
[1] Saveetha Inst Med & Tech Sci, Saveetha Med Coll & Hosp, Internal Med, Chennai, India
[2] Saveetha Inst Med & Tech Sci, Saveetha Med Coll & Hosp, Med Gastroenterol, Chennai, India
关键词
corticosteroids; eosinophilic enteritis; peripheral eosinophilia; low saag ascites; eosinophilic; gastrointestinal disorders; GASTROENTERITIS;
D O I
10.7759/cureus.68511
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Eosinophilic ascites (EA) is a rare and often challenging clinical manifestation of eosinophilic gastroenteritis (EGE), a condition characterized by eosinophilic infiltration in various layers of the gastrointestinal tract. EA specifically involves the abnormal accumulation of eosinophils in the peritoneal cavity, which can lead to significant abdominal distension and discomfort. EGE is an inflammatory disorder that can affect the mucosal, muscular, or serosal layers of the gastrointestinal tract, primarily resulting from a combination of genetic predisposition, environmental triggers, and immune responses. This case report discusses a 39-yearold male who presented with persistent abdominal distension, significant weight loss, vomiting, and chronic diarrhea. Clinical evaluation revealed marked eosinophilia and EA, prompting a series of diagnostic tests to differentiate it from other potential causes such as parasitic infections and malignancies. Imaging studies indicated moderate ascites and intestinal wall thickening. The patient was diagnosed with eosinophilic enteritis, and treatment with corticosteroids led to substantial clinical improvement. This case highlights the diagnostic challenges and management strategies associated with both EA and EGE, emphasizing the importance of recognizing these rare manifestations of eosinophilic gastrointestinal disorders.
引用
收藏
页数:9
相关论文
共 50 条
  • [41] Rare, very rare, and even rarer: carcinoid tumour, sclerosing pneumocytoma, and combined carcinoid tumour and sclerosing pneumocytoma
    Ozlu, M. S.
    Aknar, H.
    Yenigun, B. M.
    Sak, S. Dizbay
    VIRCHOWS ARCHIV, 2024, 485 : S447 - S448
  • [42] Eosinophilic Ascites: A Rare Case Report With Diagnostic and Therapeutic Challenges
    Devi, Sujata
    Kar, Nilanjan
    Sahoo, Debananda
    Dey, Anupam
    Das, Dhriti Sundar
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2020, 12 (11)
  • [43] Subserosal eosinophilic gastroenteritis with ascites - Case report of a rare disease
    Szetoo, W.
    Haikings, R.
    Boyd, P.
    Ombiga, J.
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2014, 29 : 135 - 136
  • [44] Eosinophilic gastroenteritis in a teenager: A rare diagnosis
    Masiques Mas, Lluisa
    Coll Sibina, Maria Teresa
    Sans Tojo, Josep
    Conti, Romina
    Cuatrecases, Miriam
    GASTROENTEROLOGIA Y HEPATOLOGIA, 2017, 40 (06): : 401 - 403
  • [45] Non-cirrhotic ascites: Pathophysiology, diagnosis and etiology
    Carrier, P.
    Jacques, J.
    Debette-Gratien, M.
    Legros, R.
    Sarabi, M.
    Vidal, E.
    Sautereau, D.
    Bezanahary, H.
    Ly, K. H.
    Loustaud-Ratti, V.
    REVUE DE MEDECINE INTERNE, 2014, 35 (06): : 365 - 371
  • [46] Eosinophilic ascites
    Kobayashi, TK
    Ueda, M
    Nishino, T
    Muramatsu, M
    Moritani, S
    Shigematsu, T
    Kohno, Y
    Kaneko, C
    Kushima, R
    CYTOPATHOLOGY, 2003, 14 (02) : 84 - 86
  • [47] Eosinophilic ascites
    Lin, J-C.
    Tsao, Y-T.
    Lin, S-H.
    DIGESTIVE AND LIVER DISEASE, 2008, 40 (10) : 834 - 834
  • [48] RARE OCCURRENCE: PULMONARY DIROFILARIASIS AS ETIOLOGY OF EOSINOPHILIC PLEURAL EFFUSION
    Faruqi, Muhammad Asad
    Ashraf, Obaid
    Virani, Ahmed
    Dumont, Tiffany
    CHEST, 2020, 158 (04) : 1250A - 1250A
  • [49] Rare metals getting rarer
    Ragnarsdottir, Kristin Vala
    NATURE GEOSCIENCE, 2008, 1 (11) : 720 - 721
  • [50] A Rare Fracture, an Even Rarer Treatment: The Arthroscopic Reduction and Internal Fixation of an Isolated Femoral Head Fracture
    Matsuda, Dean K.
    ARTHROSCOPY-THE JOURNAL OF ARTHROSCOPIC AND RELATED SURGERY, 2009, 25 (04): : 408 - 412