Sim Jongmin, Koh Hyun Hee, Choi Sangjoon, Chu Jinah, Kim Tae Sung, Kim Hojoong, Han Joungho
Department of Pathology and Translational Genomics, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Department of Radiology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
J Pathol Transl Med. 2018 Jul;52(4):211-218. doi: 10.4132/jptm.2018.04.27. Epub 2018 Jun 15.
Pulmonary nodular lymphoid hyperplasia (PNLH) is a non-neoplastic pulmonary lymphoid disorder that can be mistaken for malignancy on radiography. Herein, we present nine cases of PNLH, emphasizing clinicoradiological findings and histological features.
We analyzed radiological and clinicopathological features from the electronic medical records of nine patients (eight females and one male) diagnosed with PNLH. IgG and IgG4 immunohistochemical staining was performed in three patients.
Two of the nine patients had experienced tuberculosis 40 and 30 years prior, respectively. Interestingly, none were current smokers, although two were ex-smokers. Three patients complaining of persistent cough underwent computed tomography of the chest. PNLH was incidentally discovered in five patients during examination for other reasons. The remaining patient was diagnosed with the disease following treatment for pneumonia. Imaging studies revealed consolidation or a mass-like lesion in eight patients. First impressions included invasive adenocarcinoma and mucosal-associated lymphoid tissue‒type lymphoma. Aspergillosis was suspected in the remaining patient based on radiological images. Resection was performed in all patients. Microscopically, the lesions consisted of nodular proliferation of reactive germinal centers accompanied by infiltration of neutrophils and macrophages in various degrees and surrounding fibrosis. Ultimately, all nine patients were diagnosed with PNLH and showed no evidence of recurrence on follow-up.
PNLH is an uncommon but distinct entity with a benign nature, and understanding the radiological and clinicopathological characteristics of PNLH is important.
肺结节样淋巴组织增生(PNLH)是一种非肿瘤性肺淋巴组织疾病,在影像学上可能被误诊为恶性肿瘤。在此,我们报告9例PNLH病例,重点阐述临床放射学表现和组织学特征。
我们分析了9例诊断为PNLH患者(8例女性,1例男性)的电子病历中的放射学和临床病理特征。对3例患者进行了IgG和IgG4免疫组化染色。
9例患者中有2例分别在40年和30年前患过结核病。有趣的是,尽管有2例曾吸烟,但目前均不吸烟。3例主诉持续咳嗽的患者接受了胸部计算机断层扫描。5例患者在因其他原因检查时偶然发现了PNLH。其余1例患者在肺炎治疗后被诊断出患有该病。影像学检查显示8例患者有实变或肿块样病变。初步印象包括浸润性腺癌和黏膜相关淋巴组织型淋巴瘤。根据影像学图像,其余1例患者怀疑患有曲霉病。所有患者均接受了手术切除。显微镜下,病变由反应性生发中心的结节状增生组成,伴有不同程度的中性粒细胞和巨噬细胞浸润以及周围纤维化。最终,所有9例患者均被诊断为PNLH,随访期间均无复发迹象。
PNLH是一种罕见但性质明确的良性疾病,了解其放射学和临床病理特征很重要。