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一例随访20年的巨大胰腺浆液性微囊性腺瘤

A giant pancreatic serous microcystic adenoma with 20 years follow-up.

作者信息

Schulz Hans-Ulrich, Kellner Udo, Kahl Stefan, Effenberger Olaf, Asperger Walter, Lippert Hans, Röcken Christoph

机构信息

Chirurgie/Department of Surgery, University of Magdeburg, Leipziger Str. 44, 39120, Magdeburg, Germany.

出版信息

Langenbecks Arch Surg. 2007 Mar;392(2):209-13. doi: 10.1007/s00423-006-0146-1. Epub 2007 Jan 19.

Abstract

BACKGROUND AND AIMS

There is only little information about the spontaneous course of large pancreatic serous tumours. We followed up a white woman with a giant serous microcystic adenoma over more than 20 years.

CASE REPORT

At first clinical presentation, in 1986, the tumour measured 4.5 cm in diameter. Two years later, it measured 6 cm and was considered as non-resectable at laparotomy. A biopsy was obtained, and the tumour was diagnosed as lymphangioma, based on hematoxylin and eosin-staining. During the follow-up, the tumour progressively increased in size, measuring 12 cm in diameter in 1993 and 17 cm in 2000. Thus, an average growth rate of 0.83 cm per year was calculated. Unspecific abdominal discomfort and pain were the leading clinical symptoms. A colonic resection was necessary because of compression by the tumour in 1993. Portal hypertension was detected at laparotomy. Finally, the initial biopsy specimen was re-evaluated, using immunohistochemistry, and the final diagnosis of a serous microcystic adenoma was made.

CONCLUSION

This unique case demonstrates that the spontaneous course of serous microcystic adenoma of the pancreas may be favourable even with huge tumour size and that immunohistochemistry may prove a valuable tool for differential diagnosis of cystic pancreatic lesions. Due to their size and progressive, space-occupying growth, these biologically benign tumours may cause injury to adjacent organs and thus clinical symptoms. For this reason, curative surgical resection is the treatment of choice for this tumour entity except for small, asymptomatic lesions, which do not require intervention. When radical resection is impossible, palliative surgery may improve the quality of life for several years. The risk of malignant transformation seems to be low even in the long-term course.

摘要

背景与目的

关于大型胰腺浆液性肿瘤的自然病程,目前仅有少量信息。我们对一名患有巨大浆液性微囊性腺瘤的白人女性进行了20多年的随访。

病例报告

1986年首次临床表现时,肿瘤直径为4.5厘米。两年后,其直径为6厘米,在剖腹手术中被认为不可切除。获取了活检样本,基于苏木精和伊红染色,肿瘤被诊断为淋巴管瘤。在随访期间,肿瘤大小逐渐增加,1993年直径为12厘米,2000年为17厘米。因此,计算出平均每年生长速度为0.83厘米。非特异性腹部不适和疼痛是主要临床症状。1993年因肿瘤压迫进行了结肠切除术。剖腹手术时检测到门静脉高压。最后,使用免疫组织化学对最初的活检标本进行重新评估,最终诊断为浆液性微囊性腺瘤。

结论

这个独特的病例表明,即使肿瘤体积巨大,胰腺浆液性微囊性腺瘤的自然病程也可能较好,并且免疫组织化学可能是诊断胰腺囊性病变的一种有价值的工具。由于其大小和进行性的占位性生长,这些生物学上良性的肿瘤可能会对相邻器官造成损伤,从而引起临床症状。因此,除了小的无症状病变不需要干预外,根治性手术切除是这种肿瘤实体的首选治疗方法。当无法进行根治性切除时,姑息性手术可能会在几年内改善生活质量。即使在长期病程中,恶变风险似乎也较低。

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