Mesenteric Panniculitis: An Unusual Initial Presentation Of Systemic Lupus Erythematosus (SLE)
Mesenteric Panniculitis: An Unusual Initial Presentation Of Systemic Lupus Erythematosus (SLE)
复制标题
肠系膜脂膜炎:系统性红斑狼疮 (SLE) 的一种不寻常的初始表现
DOI:
10.5580/bc5
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发表时间:
2004
期刊:
影响因子:
--
通讯作者:
P. Chadha
中科院分区:
文献类型:
--
作者:
Deepak Pahuja;Manoharan W. Eustace;P. Chadha
Introduction: Patients with SLE are subject to a myriad of symptoms and complaints, and the inflammatory process can affect virtually every organ. The most common pattern of disease is a mixture of constitutional complaints with skin, musculoskeletal, hematological and serologic involvement. Mesenteric panniculitis is a rare disease affecting adipose tissue of the mesentery that may result in the development of large masses in the abdomen. Diffuse chronic or intermittent abdominal pain is the most frequent symptom. Literature Search: We performed a Medline search using panniculitis as subject heading and peritoneal and mesenteric panniculitis as additional keywords. The search yielded 142 articles. Combining this search with our second search on Systemic Lupus Erythematosus yielded only one result in a French journal of a 10 year girl with mesenteric panniculitis as initial presentation of acute lupus erythematosus. Case: We describe a 44 year old female with one year of recurrent abdominal pain and an otherwise negative past medical history. She underwent a laparoscopy for definite diagnosis of her abdominal pain. At surgery, chylous ascites was noted and a subsequent open laparotomy showed necrotic areas in the mesentery. Biopsy results revealed fat necrosis and an abdominal CT scan showed classic features of panniculitis. This patient later presented with night sweats, fever, lower extremity rash, pain in the proximal interphalyngeal joints of her left hand with swelling and decrease in range of motion and thrombocytopenia. She also complained of dryness in her eyes and ears. Subsequent workup revealed she was ANA positive with a titer of 1:1280 in a speckled pattern and positive SSA and SSB antibody. Skin biopsy showed leukocytoclastic vasculitis. In addition she had a history of two miscarriages. She was diagnosed as having systemic lupus erythematosus manifesting with secondary sjogren's and idiopathic thrombocytopenia, and was started on oral corticosteroid treatment with excellent response. Conclusion: Systemic lupus erythematosus must be included among the etiologies of intraabdominal panniculitis.