Leptomeningeal Metastases in Carcinoma Rectum with Extensive Skeletal Metastasis - A Case Report

None Chayan Paul, None Abhishek Basu, None Abhay Chakravarty
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 Colorectal cancer (CRC) is the third most common cancer diagnosed in both men and women.[1] The incidence of it has been rising in young adults.[2] The common metastatic sites of CRC include the liver (57.6%), abdominal lymph nodes (48.3%), lungs (37.6%) and Peritoneum.[3,4,5] Skeletal metastasis without other organ metastasis is very rare. Bone metastasis is seen in 4.7% to 10.9% in clinical cases and often indicates advanced disease with a poor prognosis with 5-year survival rate less than 5%,[6] leading to significantly high rate of morbidity and mortality.
 Leptomeningeal Metastases (LM) or neoplastic meningitis, is an uncommon metastatic complication of solid tumour progression. Most commonly arising from breast, non-small-cell lung cancer, and melanoma with a frequency of 5% to 25%.[7] The incidence of LM in colorectal cancer (CRC) is far less than 1%.[8]
 Here we report a case of rectal carcinoma, with extensive skeletal metastases and their pattern of bone involvement, who later presented with meningeal metastases.","PeriodicalId":47072,"journal":{"name":"Journal of Evolution of Medical and Dental Sciences-JEMDS","volume":"59 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Evolution of Medical and Dental Sciences-JEMDS","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14260/jemds.v12i10.502","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Incidence of rectal carcinoma has been rising in younger people in recent decades. Skeletal metastasis without other organ metastasis from primary rectal carcinoma is very rare, spine and the pelvis are the first sites of bony metastasis. Leptomeningeal Metastases (LM) is a very rare complication of solid tumour progression and its incidence in colorectal carcinoma is far less. A nineteen-year-old male presented in the OPD with rectal bleeding and low back pain with colonoscopic biopsy proving rectal carcinoma. MRI of pelvis revealed multiple osseous metastases to vertebrae and pelvic bones. After four cycles of palliative chemotherapy, he developed lower back pain. Repeat MRI revealed multiple lesions in the vertebrae and long bones for which he received palliative external beam radiation therapy (EBRT). Subsequently seven months later he developed meningeal metastases and received whole brain radiation and supportive care. LM in patients with primary colorectal cancer (CRC) remains an exceedingly rare complication of metastatic disease progression in CRC. Colorectal cancer (CRC) is the third most common cancer diagnosed in both men and women.[1] The incidence of it has been rising in young adults.[2] The common metastatic sites of CRC include the liver (57.6%), abdominal lymph nodes (48.3%), lungs (37.6%) and Peritoneum.[3,4,5] Skeletal metastasis without other organ metastasis is very rare. Bone metastasis is seen in 4.7% to 10.9% in clinical cases and often indicates advanced disease with a poor prognosis with 5-year survival rate less than 5%,[6] leading to significantly high rate of morbidity and mortality. Leptomeningeal Metastases (LM) or neoplastic meningitis, is an uncommon metastatic complication of solid tumour progression. Most commonly arising from breast, non-small-cell lung cancer, and melanoma with a frequency of 5% to 25%.[7] The incidence of LM in colorectal cancer (CRC) is far less than 1%.[8] Here we report a case of rectal carcinoma, with extensive skeletal metastases and their pattern of bone involvement, who later presented with meningeal metastases.
直肠轻脑膜转移伴广泛骨转移1例
近几十年来,年轻人直肠癌的发病率一直在上升。摘要原发性直肠癌骨转移而无其他器官转移是非常罕见的,脊柱和骨盆是骨转移的首要部位。轻脑膜转移是一种非常罕见的实体瘤进展并发症,其在结直肠癌中的发病率要低得多。一个19岁的男性在门诊提出直肠出血和腰痛与结肠镜活检证实直肠癌。骨盆MRI显示多发性骨转移到椎骨和骨盆骨。经过四个周期的姑息性化疗后,他出现了腰痛。重复MRI显示椎骨和长骨多发病变,他接受了姑息性外束放射治疗(EBRT)。7个月后,他出现脑膜转移,接受全脑放疗和支持性治疗。原发性结直肠癌(CRC)患者的LM仍然是CRC转移性疾病进展的极其罕见的并发症。 结直肠癌(CRC)是男性和女性中第三大最常见的癌症。[1]它在年轻人中的发病率一直在上升。[2]结直肠癌的常见转移部位包括肝脏(57.6%)、腹部淋巴结(48.3%)、肺部(37.6%)和腹膜。[3,4,5]骨骼转移而无其他器官转移是非常罕见的。骨转移在临床病例中占4.7% ~ 10.9%,常为疾病晚期,预后较差,5年生存率不足5%[6],导致发病率和死亡率显著增高。 脑膜轻脑膜转移(LM)或肿瘤性脑膜炎,是一种罕见的转移性并发症的实体瘤进展。最常见于乳腺癌、非小细胞肺癌和黑色素瘤,发病率为5%至25%。[7]LM在结直肠癌(CRC)中的发病率远低于1% [8] 在这里,我们报告一例直肠癌,与广泛的骨骼转移和他们的骨累及模式,谁后来提出了脑膜转移。
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