Nodular histiocytic/mesothelial hyperplasia (NHMH) is a benign localized alteration, firstuddescribed in 1975 by Rosai in the hernia sac [1]. Few pulmonary cases have been reported in literatureud[2–6]. Sometimes it has been reported in the pericardium [7,8] or presenting as an inguinaludmass [9]. The ‘mesothelial/monocytic incidental cardiac excrescence’, first described by Weinot et al.udin 1994 [10] is now considered a similar lesion to NHMH [11].udIt consists of a reactive proliferation of histiocytes and mesothelium secondary to chronic irritationudand it has been observed in pleura-damaging processes, such as pneumothorax [5], or as consequenceudof cardiac catheterization, inflammation, mechanical or tumor stimulation [11].udThe rarity of NHMH and the moderate cytological atypia often present, make this lesion difficultudto diagnose. It can be easily confused with primary mesothelial lesions and neoplasms suchudas adenocarcinomas, granulosa cell tumors or Langerhans’ histiocytosis.udWe report a case of pleural NHMH in a patient with a subphrenic abscess, in which no pulmonaryudpathogenic noxa was evident. We hypothesize a transdiaphragmatic chronic irritation as audpathogenetic mechanism underlying NHMH.
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机译:结节性组织细胞增生/间皮增生(NHMH)是一种良性局限性改变,于1975年由Rosai在疝囊中首次描述[1]。文献中很少报道肺部疾病 ud [2-6]。有时已在心包[7,8]或腹股沟肿块[9]中报道。 Weinot等人[udin 1994 [10]首先描述的“间皮/单核细胞偶发性心脏衰竭”现在被认为与NHMH [11]类似。 ud它由慢性刺激后组织细胞和间皮的反应性增殖组成。 udd已在胸膜破坏过程中观察到,例如气胸[5]或因心脏导管插入,炎症,机械或肿瘤刺激而导致的结果[11]。 ud NHMH的罕见性和中等程度的细胞学非典型性使这个病变难以诊断。它很容易与原发性间皮病变和肿瘤混和,如:腺癌,颗粒细胞瘤或朗格汉斯组织细胞增生。我们假设跨dia肌的慢性刺激是NHMH的成因机制。
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