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小细胞肺癌与原发性直肠去分化脂肪肉瘤伴骨样分化的同时发生:一例罕见病例报告。

Synchronous occurrence of small cell lung cancer and primary rectal dedifferentiated liposarcoma with osteosarcomatous differentiation: A rare case report.

机构信息

Department of Pathology, Henan University attached Nanyang first people Hospital, Nanyang, Henan Province, China.

出版信息

Medicine (Baltimore). 2023 Sep 29;102(39):e35465. doi: 10.1097/MD.0000000000035465.

Abstract

RATIONALE

Rectal dedifferentiated liposarcoma (DDL) and DDL with osteosarcomatous differentiation both are extremely unwonted. In addition, there are no reports of simultaneous DDL with osteosarcoma differentiation with small cell lung cancer (SCLC) to date. Therefore, it is imperative to alert clinicians and pathologists to this extremely rare and instructive synchronous tumor.

PATIENT CONCERNS

The patient was a 63-year-old male who presented with intermittent hematochezia and a swelling in the anus. Irregular masses were found on computed tomography (CT) examinations of the chest and abdomen respectively.

DIAGNOSIS

The final diagnosis of synchronous occurrence of SCLC and primary rectal DDL with osteosarcomatous differentiation was established by radiological, histological, immunohistochemical and molecular findings.

INTERVENTIONS

The patient underwent a puncture biopsy of the right lung mass and a complete resection of the rectal mass.

OUTCOMES

The patient abandoned treatment, and multiple SCLC metastases appeared multiple metastasis 8 months after the operation. In the end, he expired suddenly due to severe cerebral hemorrhage caused by brain SCLC metastasis.

LESSONS

DDL with osteosarcoma differentiation is infrequent, and its accurate diagnosis is based on morphology, immunohistochemistry and the necessary molecular tests. In rare cases, DDL occurs concurrently with other malignancies and and will be a challenge for pathologists and clinicians at this time. Accordingly, a comprehensive examination to identify possible synchronous tumors is very important in clinical practice.

摘要

背景

直肠去分化脂肪肉瘤(DDL)和具有骨肉瘤分化的 DDL 均极为罕见。此外,迄今为止尚无同时具有骨肉瘤分化的 DDL 合并小细胞肺癌(SCLC)的报道。因此,提醒临床医生和病理学家注意这种极其罕见且具有教学意义的同时性肿瘤至关重要。

病例介绍

患者为 63 岁男性,表现为间歇性血便和肛门肿胀。胸部和腹部的计算机断层扫描(CT)检查分别发现不规则肿块。

诊断

通过影像学、组织学、免疫组织化学和分子发现,最终诊断为 SCLC 和原发性直肠 DDL 伴骨肉瘤分化的同时发生。

干预措施

患者接受了右肺肿块的穿刺活检和直肠肿块的完全切除。

结果

患者放弃治疗,手术后 8 个月出现多处 SCLC 转移。最终,由于脑 SCLC 转移导致严重脑出血,他突然去世。

教训

具有骨肉瘤分化的 DDL 并不常见,其准确诊断基于形态学、免疫组织化学和必要的分子检测。在极少数情况下,DDL 与其他恶性肿瘤同时发生,此时将对病理学家和临床医生构成挑战。因此,在临床实践中,全面检查以确定可能的同时性肿瘤非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f287/10545380/5f133127930c/medi-102-e35465-g001.jpg

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