Department of Radiology, The Affiliated Hospital of Qingdao University, Qingdao, 266003, China.
World J Surg Oncol. 2021 May 10;19(1):146. doi: 10.1186/s12957-021-02261-y.
This study aimed to identify the characteristic radiological signs for the diagnosis of Langerhans cell histiocytosis (LCH) of the bone.
We retrospectively studied 82 cases of LCH with bone lesions confirmed by pathology. Clinical and radiological features of the patients were analyzed.
A total of 64 and 18 patients had single and multiple bone lesions, respectively. With regard to LCH with single bone lesions, 37.5% (24/64) of lesions were located in the skull and presented as bone destruction with or without soft tissue mass. The correct diagnosis rate of these lesions was 60.0% (9/15) in children and adolescents, but was only 22.2% (2/9) in adults. A total of 26.5% (17/64) of the solitary lesions were found in the spine. Of these, 88.2% (15/17) were located in the vertebral body and appeared to have different degrees of collapse, and 66.7% (10/15) of these lesions were correctly diagnosed. Of the unifocal lesions, 21.8% (14/64) were located in other flat and irregular bones and manifested as osteolysis. Only 21.4% (3/14) of these cases were correctly diagnosed. In total, 14.1% (9/64) of the isolated bone LCH lesions were located in the long bones. Of these, 77.8% (7/9) were located in the diaphysis and presented as central bone destruction with or without fusiform periosteal reaction and extensive peripheral edema, of which 42.9% (3/7) were correctly diagnosed before surgery or biopsy. With regard to LCH with multiple bony destructive lesions, 71.4% (10/14) of cases in children and adolescents were correctly diagnosed; however, all four cases among adults were misdiagnosed.
In all age groups, isolated diaphyseal destruction of the long bone with fusiform periosteal reaction and extensive peripheral edema, vertebra plana of the spine, and bevelled edge of skull defects accompanied by soft tissue masses strongly suggest LCH diagnosis. Moreover, the multiple bone osteolytic destruction in children and adolescents strongly suggests LCH diagnosis. Familiarity with these typical radiological signs of LCH is necessary to decrease misdiagnoses.
本研究旨在确定用于诊断骨朗格汉斯细胞组织细胞增生症(LCH)的特征性影像学征象。
我们回顾性研究了 82 例经病理证实有骨病变的 LCH 患者。分析了患者的临床和影像学特征。
共有 64 例和 18 例患者分别有单发和多发骨病变。对于单发骨病变的 LCH,37.5%(24/64)的病变位于颅骨,表现为伴有或不伴有软组织肿块的骨破坏。这些病变在儿童和青少年中的正确诊断率为 60.0%(9/15),但在成年人中仅为 22.2%(2/9)。64 例单发病变中有 26.5%(17/64)位于脊柱。其中,88.2%(15/17)位于椎体,表现为不同程度的塌陷,10/15 例的诊断正确。在单发病变中,21.8%(14/64)位于其他扁平不规则骨,表现为溶骨性破坏。这些病变中只有 21.4%(3/14)的诊断正确。孤立性骨 LCH 病变中,14.1%(9/64)位于长骨。其中,77.8%(7/9)位于骨干,表现为中央骨破坏,伴有或不伴有梭形骨膜反应和广泛的周围水肿,其中 42.9%(3/7)术前或活检前诊断正确。对于多发性骨破坏性病变的 LCH,儿童和青少年中的 71.4%(10/14)例的诊断正确;然而,成人中的所有 4 例均误诊。
在所有年龄组中,孤立的骨干梭形骨膜反应和广泛的周围水肿、脊柱椎体平板状改变以及颅骨缺损伴软组织肿块强烈提示 LCH 诊断。此外,儿童和青少年多发性骨溶骨性破坏强烈提示 LCH 诊断。熟悉 LCH 的这些典型影像学征象有助于减少误诊。