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Duodenal pseudomelanosis (pseudomelanosis duodeni): a rare endoscopic finding

机译:十二指肠假黑色素病(pseudomelanosis duodeni):罕见的内镜检查发现

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Duodenal pseudomelanosis (or pseudomelanosis duodeni) is a rare benign condition characterized by black-brown speckled pigmentation of the duodenal mucosa. Collections of pigment?laden macrophages are found in the tips of duodenal villi. The pigment is thought to be mostly composed of ferrous sulfide. Histochemichal stains for iron (Perl’s prussian blue) or melanin (Masson- Fontana) may be positive, but are usually negative or unpredictable. Duodenal pseudomelanosis occurs predominantly in middle-aged to old adults and more commonly in females. It is associated with chronic renal failure, arterial hypertension, diabetes mellitus and gastrointestinal bleeding. Medications such as ferrous sulfate, hydralazine, propranolol, hydrochlorothiazide and furosemide are thought to play a role as well. We report a case of a 86-year-old female who presented with a history of watery diarrhea and melena. The patient had a history of high blood pressure and ischemic stroke episodes. She was on multiple medication including hidralazine, captopril, hydrochlorthiazide and aspirin. She was dehydrated, her blood pressure was 96 × 60 mmHg and neurologic examination showed complete left hemiplegia with central VII nerve palsy. Laboratory tests showed normal serum electrolytes and renal function. Hemoglobin level was 10.7 g%. An upper endoscopy showed multiple diminutive black spots throughout the distal duodenal bulb and second portion. Histology showed multiple foci of a brown-black granular pigment inside macrophages within the tips of the villi (pseudomelanosis). Stains for iron and melanin were negative. She was treated with omeprazol, parenteral fluid replacement with saline and partial fasting. After complete recovery she was discharged for ambulatory follow up.
机译:十二指肠假黑变病(或称十二指肠黑变病)是一种罕见的良性疾病,其特征是十二指肠粘膜呈黑褐色斑点状色素沉着。在十二指肠绒毛的尖端发现有色素的巨噬细胞的集合。据认为该颜料主要由硫化亚铁组成。铁(Perl的普鲁士蓝)或黑色素(Masson-Fontana)的组织化学染色可能是阳性的,但通常是阴性或不可预测的。十二指肠假黑变病主要发生在中年至老年人,更常见于女性。它与慢性肾功能衰竭,动脉高压,糖尿病和胃肠道出血有关。药物如硫酸亚铁,肼屈嗪,普萘洛尔,氢氯噻嗪和呋塞米也被认为也起作用。我们报告一例86岁女性,曾有水样腹泻和黑便病史。该患者有高血压病史和缺血性中风发作史。她正在接受多种药物治疗,其中包括Hidralazine,Captopril,hydrochlorthiazide和aspirin。她脱水,血压为96×60 mmHg,神经系统检查显示完全偏瘫并伴有中枢VII神经麻痹。实验室检查显示血清电解质和肾功能正常。血红蛋白水平为10.7g%。上消化道内窥镜检查显示整个十二指肠球远端和第二部分有多个小的黑色斑点。组织学显示,绒毛尖端内的巨噬细胞内有棕黑色颗粒状色素的多个病灶(假单胞菌病)。铁和黑色素的污渍为阴性。她接受奥美拉唑治疗,肠胃外补液和生理盐水部分禁食。完全康复后,她出院接受门诊随访。

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