Vujanić G M, Berry P J, Frank J D
Department of Paediatric Pathology, Bristol Royal Hospital for Sick Children, United Kingdom.
Pediatr Pathol. 1992 Jul-Aug;12(4):557-61. doi: 10.3109/15513819209024206.
Inflammatory pseudotumor (IPT) of the kidney is a very rare lesion. We describe an 8-year-old boy with IPT of the kidney presenting as a single episode of hematuria. The case highlights a new feature, metaplastic bone, not previously described in IPT. This new feature may be helpful in establishing the correct preoperative and histopathologic diagnosis of IPT of kidney and avoiding inappropriately aggressive therapy. Despite its rarity, IPT of the kidney should be kept in mind in the differential diagnosis of a solitary renal mass.
肾脏炎性假瘤（IPT）是一种非常罕见的病变。我们描述了一名8岁患有肾脏IPT的男孩，其表现为单次血尿发作。该病例突出了一个新特征，即化生骨，这在以前的IPT中未曾描述过。这一新特征可能有助于建立正确的肾脏IPT术前诊断和组织病理学诊断，并避免不适当的积极治疗。尽管肾脏IPT罕见，但在孤立性肾肿块的鉴别诊断中应予以考虑。
