Shamsuzzaman S M, Hashiguchi Y
Department of Parasitology, Faculty of Medicine, Kochi Medical School, Nankoku City, Kochi 783-8505, Japan.
Clin Chest Med. 2002 Jun;23(2):479-92. doi: 10.1016/s0272-5231(01)00008-9.
Pleuropulmonary amebiasis is the common and pericardial amebiasis the rare form of thoracic amebiasis. Low socioeconomic conditions, malnutrition, chronic alcoholism, and ASD with left to right shunt are contributing factors to the development of pulmonary amebiasis. Although no age is exempt, it commonly occurs in patients aged 20 to 40 years, with an adult male to female ratio of 10:1. Children rarely develop thoracic amebiasis: when it does occur there is an equal sex distribution. The infection usually spreads to the lungs by extension of an amebic liver abscess. Infection may pass to the thorax directly from the primary intestinal lesion through hematogenous spread, however. Lymphatic spread is one possible route. Inhalation of dust containing cysts and aspiration of cysts or trophozoites of E histolytica in the lungs are some other hypothetical routes. The lung is the second most common extraintestinal site of amebic involvement after the liver. Usually the lower lobe, and sometimes the middle lobe of the right lung, are affected, but it may affect any lobe of the lungs. The patient develops fever and right upper quadrant pain that is referred to the tip of the right shoulder or in between the scapula. Hemophtysis is common. The diagnosis of thoracic amebiasis is suggested by the combination of an elevated hemidiaphragm (usually right), hepatomegaly, pleural effusion, and involvement of the right lung base in the form of haziness and obliteration of costophrenic and costodiaphragmatic angles. Infection is usually extended to the thorax by perforation of a hepatic abscess through the diaphragm and across an obliterated pleural space, producing pulmonary consolidation, abscesses, or broncho-hepatic fistula. Empyema develops when a liver abscess ruptures into the pleural space. Rarely, a posterior amebic liver abscess can burst into the inferior vena cava and develop an embolism of the inferior vena cava and thromboembolic disease of the lungs with congestive cardiac failure or corpulmonale. Diagnosis by finding E histolytica in stool specimens is of limited value. In a limited number of cases amebae might be found in aspirated pus or expectorated sputum. "Anchovy sauce-like" pus or sputum may be found. Presence of bile in sputum indicates that the pus is of liver origin. Serological tests are of immense value in diagnosis. Liver enzymes are usually normal and neutrophilic leucocytosis may or may not be found. ESR is invariably elevated. Anti-amebic antibodies can be detected by ELISA, IFAT, and IHA. Amebic antigen can be detected from serum and pus by ELISA. Detection of Entamoeba DNA in pus or sputum may be a sensitive and specific method. Pleuropulmonary amebiasis is easily confused with other illnesses and is treated as pulmonary TB, bacterial lung abscesses, and carcinoma of the lung. A single drug regimen with metronidazole with supportive therapy usually cures patients without residual anomalies. Aspiration of pus from empyema thoracis may be needed for confirmation and therapeutic purposes. The pericardium is usually involved by direct extension from the amebic abscess of the left lobe of the liver, sometimes from the right lobe of the liver, and rarely from the lungs or pleura. An initial accumulation of serous fluid due to reactive pericarditis followed by intrapericardial rupture may develop either (1) acute onset of severe symptoms with chest pain, dyspnea, and cardiac tamponade, shock, and death, or (2) progressive effusion with thoracic cage pain, progressive dyspnea, and fever. Chest radiograph, ultrasound examination, and CT scan usually confirm the presence of a liver abscess in continuity with the pericardium and fluid within the pericardial sac with or without the fistulous tract. Echocardiography may demonstrate fluid in the pericardial cavity. Patients should be cared for in the ICU and ambecides should be started without delay. Pericardiocentesis usually confirms the diagnosis and improves the general condition of the patient. Aspiration of the accumulated fluid should be performed urgently in cardiac tamponade; repeated aspiration may be needed. Surgical drainage should be done if needed. Acanthamoeba, a free-living ameba, may also infect the lungs in the form of pulmonary nodular infiltration and pulmonary edema in association with amebic meningoencephalitis in immunocompromised patients. It usually spreads to the meninges of the brain by way of the blood from its primary lesion in the lung or skin. Early diagnosis and institution of treatment may be life saving for these patients. A literature review shows that HIV/AIDS patients are not prone to infection with E histolytica. It is now clear that there are an increasing number of HIV-seropositive patients among amebic liver abscess patients, however, which suggests that although the incidence of intestinal infection is not high among HIV-seropositive or AIDS patients they are more susceptible to an invasive form of the disease.
胸膜肺阿米巴病是胸段阿米巴病的常见类型,心包阿米巴病则较为罕见。社会经济条件差、营养不良、慢性酒精中毒以及左向右分流的房间隔缺损是肺阿米巴病发生的促成因素。虽然各年龄段均可发病,但该病常见于20至40岁的患者,成年男性与女性的比例为10:1。儿童很少发生胸段阿米巴病:若发病,男女发病率相等。感染通常通过阿米巴肝脓肿的蔓延扩散至肺部。不过,感染也可能通过血行播散从原发性肠道病变直接蔓延至胸部。淋巴扩散也是一种可能的途径。吸入含有包囊的灰尘以及肺内吸入溶组织内阿米巴的包囊或滋养体是其他一些可能的途径。肺是继肝脏之后阿米巴累及的第二常见肠外部位。通常下叶,有时右肺中叶会受到影响,但也可能累及肺的任何叶。患者会出现发热和右上腹疼痛,疼痛可放射至右肩尖或肩胛之间。咯血很常见。胸段阿米巴病的诊断依据包括半侧膈肌抬高(通常为右侧)、肝肿大、胸腔积液以及右肺底部出现模糊影和肋膈角及肋膈窦消失等表现。感染通常通过肝脓肿穿破膈肌并跨越闭塞的胸膜腔蔓延至胸部,导致肺实变、脓肿或支气管 - 肝瘘。当肝脓肿破入胸膜腔时会形成脓胸。罕见情况下,肝后阿米巴脓肿可破入下腔静脉,引发下腔静脉栓塞和肺部血栓栓塞性疾病,并伴有充血性心力衰竭或肺心病。通过在粪便标本中发现溶组织内阿米巴进行诊断的价值有限。在少数病例中,可在吸出的脓液或咳出的痰液中发现阿米巴。可能会发现“鱼酱样”脓液或痰液。痰液中存在胆汁表明脓液来自肝脏。血清学检测在诊断中具有重要价值。肝酶通常正常,可能会出现或不出现中性粒细胞增多。血沉总是升高。可通过酶联免疫吸附测定(ELISA)、间接荧光抗体试验(IFAT)和间接血凝试验(IHA)检测抗阿米巴抗体。可通过ELISA从血清和脓液中检测阿米巴抗原。在脓液或痰液中检测溶组织内阿米巴DNA可能是一种敏感且特异的方法。胸膜肺阿米巴病容易与其他疾病混淆,常被误诊为肺结核、细菌性肺脓肿和肺癌。采用甲硝唑单一药物治疗方案并辅以支持治疗通常可治愈患者且无残留异常。为了确诊和治疗,可能需要抽吸胸腔积脓。心包通常通过肝左叶的阿米巴脓肿直接蔓延受累,有时也可由肝右叶蔓延所致,很少由肺或胸膜蔓延引起。最初因反应性心包炎导致浆液性液体积聚,随后心包内破裂,可能会出现以下两种情况:(1)突然出现严重症状,伴有胸痛、呼吸困难、心脏压塞、休克和死亡;(2)逐渐出现胸腔疼痛、进行性呼吸困难和发热。胸部X线、超声检查和CT扫描通常可证实存在与心包相连的肝脓肿以及心包腔内有液体,有无瘘管均可发现。超声心动图可能显示心包腔内有液体。患者应在重症监护病房接受治疗,并应立即开始使用甲硝唑。心包穿刺通常可确诊并改善患者的一般状况。对于心脏压塞患者,应紧急抽吸积聚的液体;可能需要反复抽吸。如有必要,应进行手术引流。棘阿米巴,一种自由生活的阿米巴,在免疫功能低下的患者中,可能以肺结节浸润和肺水肿的形式感染肺部,并伴有阿米巴脑膜脑炎。它通常从肺部或皮肤的原发性病变通过血液传播至脑膜。早期诊断和治疗对这些患者可能挽救生命。文献综述表明,人类免疫缺陷病毒/获得性免疫综合征(HIV/AIDS)患者不易感染溶组织内阿米巴。然而,目前很清楚地发现,在阿米巴肝脓肿患者中,HIV血清阳性患者的数量在增加,这表明尽管HIV血清阳性或艾滋病患者的肠道感染发生率不高,但他们更容易发生侵袭性疾病。