胰腺腺泡细胞癌伴皮下脂膜炎

Acinar cell carcinoma of the pancreas associated with subcutaneous panniculitis.

作者信息

Moro Margherita, Moletta Lucia, Blandamura Stella, Sperti Cosimo

机构信息

Fourth Surgical Clinic, Department of Surgery, University of Padua, Padua, Italy.

出版信息

JOP. 2011 May 6;12(3):292-6.

DOI:
Abstract

CONTEXT

Acinar cell carcinoma is a rare pancreatic malignant tumor, which can be associated with a particular manifestation: pancreatic panniculitis. It presents with erythematous subcutaneous nodules located mainly on the legs. The skin lesions can precede, be concurrent with or follow the pancreatic illness. The pathogenesis is not fully understood, but it is believed to be associated with high levels of serum lipase produced by the neoplasm, causing fat necrosis in tissues. The treatment of pancreatic panniculitis is directed at the underlying pancreatic disease, which may result in regression of the skin lesions. We report a case of pancreatic acinar cell carcinoma associated with subcutaneous panniculitis together with a review of the English literature.

CASE REPORT

A 79-year-old woman, with a 13-month history of acute pancreatitis, asthenia, weight loss, and the CT finding of a mass in the pancreatic head, presented complaining of multiple, migrant and painful subcutaneous nodules on her lower extremities. High serum lipase levels were also present. She underwent a pancreaticoduodenectomy, with subsequent regression of the skin lesions and normalization of her serum lipase levels. Histology revealed an acinar cell carcinoma of the pancreas. Liver metastases occurred six months after surgery, and the patient underwent chemotherapy with gemcitabine. She is still alive 14 months after the initial surgery.

CONCLUSIONS

Although rare, the association between acinar cell carcinoma and pancreatic panniculitis has been described in the literature. In a patient with subcutaneous nodules, the presence of acinar cell carcinoma should be considered in order to prevent long delays in the diagnosis and treatment of this pancreatic malignancy.

摘要

背景

腺泡细胞癌是一种罕见的胰腺恶性肿瘤,可伴有一种特殊表现:胰腺性脂膜炎。其表现为主要位于腿部的红斑性皮下结节。皮肤病变可先于胰腺疾病出现、与胰腺疾病同时出现或在胰腺疾病之后出现。发病机制尚未完全明确,但据信与肿瘤产生的高水平血清脂肪酶有关,导致组织脂肪坏死。胰腺性脂膜炎的治疗针对潜在的胰腺疾病,这可能导致皮肤病变消退。我们报告一例伴有皮下脂膜炎的胰腺腺泡细胞癌病例,并对英文文献进行综述。

病例报告

一名79岁女性,有13个月的急性胰腺炎病史、乏力、体重减轻,CT检查发现胰头有肿块,主诉下肢有多个游走性疼痛性皮下结节。血清脂肪酶水平也升高。她接受了胰十二指肠切除术,随后皮肤病变消退,血清脂肪酶水平恢复正常。组织学检查显示为胰腺腺泡细胞癌。术后6个月出现肝转移,患者接受了吉西他滨化疗。初次手术后14个月她仍然存活。

结论

尽管罕见,但腺泡细胞癌与胰腺性脂膜炎之间的关联在文献中已有描述。对于有皮下结节的患者,应考虑腺泡细胞癌的存在,以避免这种胰腺恶性肿瘤的诊断和治疗出现长时间延误。

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