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Hepatic granulomas associated with brucellosis

机译:与布鲁氏菌病相关的肝肉芽肿

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Brucellosis, a bacterial disease caused by members of the ge-nus Brucella, remains one of the most common zoonotic dis-eases worldwide (1-3). The disease occurs in both animals and humans, except in those countries where bovine Brucellosis has been eradicated (1). The bacterial pathogen is classified by the CDC as a category-B pathogen that has potential for develop-ment as a bioterrorist agent (1, 4). Brucella spp. is considered to be the most common laboratory-acquired pathogen (1, 5). In hu-mans, Brucellosis behaves as a systemic infection with a very het-erogeneous clinical spectrum (2, 3, 6). The Brucella organism's predilection for organs rich in reticuloendothelial cells (spleen, liver, bone marrow, lymph nodes) and its intracellular location are responsible for the chronicity of the disease, which can last for months or even years (1, 2, 7). Brucella has been reported to compromise the central and peripheral nervous system, as well as the gastrointestinal, hepatobiliary, genitourinary, musculo-skeletal, cardiovascular, and integumentary systems (2). In pa-tients with Brucellosis, the gastrointestinal system is commonly compromised (70%) (5). Because the liver is the largest organ of the reticuloendothelial system and plays the important role of defense mechanism against Brucella infections, diffuse hepatic involvement is usually recorded during the course of human Brucellosis infection (8). Brucellosis involves the liver in varying ways, including a slight increase in transaminase levels, mild hepatosplenomegaly, chronic suppurative disease, and, more rarely, acute hepatitis (5, 8-13). In patients infected with Brucella melitensis, the involvement of bile canals is observed more of-ten than other Brucellosis factors (14). Hepatic granulomas are often encountered during liver biopsy and can be caused by a variety of conditions such as a primary hepatic process, fever of unknown origin, or a manifestation of a systemic illness (15, 16). Granulomas are reportedly present in 2 to 10% of all liver-biopsy specimens examined in general practice (17). Liver Brucelloma, or pseudotumoral necrotizing granuloma, is an uncommon type of hepatic manifestation by Brucella and is observed in only 1.7% of patients affected by Brucellosis (8). Hepatic Brucel-loma is rarely the first to manifest itself clinically, and a focal suppurative lesion may occur if acute Brucellosis is undetected or undertreated in the patient (18). Granulomas are aggregates of macrophages, often admixed with other inflammatory cells, which usually result from a chronic presence of antigens. Gran-ulomas are a unique inflammatory response that may be idio-pathic or may be a response to a bacterial, fungal, viral, or para-sitic infection, in the latter cases representing a manifestation of underlying malignancy (15, 17).The pathology report on Bru-celloma usually shows necrotizing granulomas with a periph-eral halo of epithelioid cells. lymphocytes, and plasma cells, as well as and a polimorphonuclear infiltrate in the necrotic area (19-21). Brucellosis involving Brucella abortus is the most com-mon species that can cause hepatic granulomas that are indis-tinguishable from sarcoidosis (13, 16), and Brucella abortus is the most common species that can cause hepatic granulomas.
机译:布鲁氏菌病是一种由布鲁氏杆菌属引起的细菌性疾病,仍然是全世界最常见的人畜共患病之一(1-3)。该疾病在动物和人类中均会发生,但在已根除牛布鲁氏菌病的国家中除外(1)。 CDC将细菌病原体归类为B类病原体,具有发展成为生物恐怖分子的潜力(1、4)。布鲁氏菌属。被认为是最常见的实验室获得性病原体(1、5)。在人类中,布鲁氏菌病表现为系统性感染,临床谱非常异类(2、3、6)。布鲁氏菌对富含网状内皮细胞(脾,肝,骨髓,淋巴结)的器官的偏爱及其在细胞内的位置决定了该病的慢性,这种病可持续数月甚至数年(1、2、7)。据报道,布鲁氏菌会损害中枢和周围神经系统,以及胃肠道,肝胆,泌尿生殖系统,肌肉骨骼,心血管和外皮系统(2)。在布鲁氏菌病患者中,胃肠系统通常受到损害(70%)(5)。由于肝脏是网状内皮系统的最大器官,并且在对抗布鲁氏菌感染中起着重要的防御作用,因此在人类布鲁氏菌病感染过程中通常会记录到弥漫性肝脏受累(8)。布鲁氏菌病以各种不同的方式累及肝脏,包括转氨酶水平的轻微升高,轻度肝脾肿大,慢性化脓性疾病,以及罕见的急性肝炎(5、8-13)。在感染布鲁氏菌的患者中,与其他布鲁氏菌病因素相比,经常观察到胆管受累的可能性更高(14)。肝肉芽肿通常在肝活检期间遇到,并且可能由多种情况引起,例如原发性肝过程,不明原因的发烧或全身性疾病的表现(15、16)。据报道,在常规检查中,肉芽肿占所有肝活检标本的2%至10%(17)。肝布鲁氏细胞瘤或假瘤坏死性肉芽肿是布鲁氏菌病罕见的肝表现类型,仅在1.7%的布鲁氏菌病患者中观察到(8)。肝Brucel-loma很少在临床上首先表现出来,如果在患者中未发现或未治疗急性Brucellosis,可能会发生局灶性化脓性病变(18)。肉芽肿是巨噬细胞的聚集体,通常与其他炎性细胞混合,这通常是由于长期存在抗原引起的。肉芽肿是一种独特的炎症反应,可能是特发性的,也可能是对细菌,真菌,病毒或寄生虫感染的反应,在后一种情况下代表潜在的恶性肿瘤表现(15,17)。布鲁氏细胞瘤的病理报告通常显示坏死性肉芽肿,伴有上皮样细胞的周围光晕。坏死区域浸润了淋巴细胞,浆细胞以及多形核(19-21)。涉及流产布鲁氏菌的布鲁氏菌病是最常见的可引起肝肉芽肿,与结节病难以区分的物种(13、16),而布鲁氏菌流产是可引起肝肉芽肿的最常见物种。

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