Reynard Maxence Emmanuel, Strati Titika-Marina, Egger Bernhard
Department of Surgery, HFR Fribourg - Cantonal Hospital, Chemin des Pensionnats 2-6, 1752 Villars-sur-Glâne, Switzerland.
Department of Surgery, HFR Fribourg - Cantonal Hospital, Chemin des Pensionnats 2-6, 1752 Villars-sur-Glâne, Switzerland.
Int J Surg Case Rep. 2023 Aug;109:108599. doi: 10.1016/j.ijscr.2023.108599. Epub 2023 Aug 2.
Primary and metastatic carcinoma of the small intestine are rare. While most of these malignancies are adenocarcinomas, squamous cell carcinoma (SCC) of the gastrointestinal tract is uncommon. We present a case report of a rare occurrence of skin SCC metastasizing to the ileum, highlighting diagnostic challenges and clinical implications.
An 83-year-old female had a history of cutaneous SCC excision in the right temporal region two years prior to the current emergency department visit, followed by metastatic recurrence in a right intra-parotid lymph node treated with radiotherapy. The patient exhibited septic shock and an acute abdomen, and an abdominal computed tomography scan revealed signs of intestinal perforation. Emergency exploratory laparotomy confirmed purulent peritonitis and perforation of the terminal ileum. Subsequently, a 20 cm intestinal resection was performed. Histopathological examination of the resected specimen revealed a 4 cm perforated SCC of the small intestine (pT4 pN0 L0 V1 Pn0 R0).
Metastases of the small intestine are rare. The primary sites for these metastases are typically the uterus, cervix, colon, lung, breast, or melanoma. SCC of the small intestine is particularly rare and poses challenges in diagnosis owing to non-specific symptoms. The prognosis for SCC of the small intestine is generally poor, and the potentially aggressive behavior of some skin SCC emphasizes the need for increased awareness and vigilance in managing such cases.
This case report underscores the importance of considering metastatic disease in the small bowel of patients with a history of skin SCC who present with new-onset abdominal symptoms.
小肠原发性癌和转移性癌均较为罕见。虽然这些恶性肿瘤大多为腺癌,但胃肠道鳞状细胞癌(SCC)并不常见。我们报告一例罕见的皮肤SCC转移至回肠的病例,强调诊断挑战及临床意义。
一名83岁女性,在本次急诊就诊前两年有右侧颞部皮肤SCC切除史,随后右侧腮腺内淋巴结出现转移性复发并接受放疗。患者出现感染性休克和急腹症,腹部计算机断层扫描显示肠道穿孔迹象。急诊剖腹探查证实为化脓性腹膜炎和回肠末端穿孔。随后进行了20厘米的肠切除术。切除标本的组织病理学检查显示为小肠4厘米穿孔性SCC(pT4 pN0 L0 V1 Pn0 R0)。
小肠转移罕见。这些转移的原发部位通常是子宫、宫颈、结肠、肺、乳腺或黑色素瘤。小肠SCC尤为罕见,因其症状不具特异性,在诊断上存在挑战。小肠SCC的预后通常较差,一些皮肤SCC的潜在侵袭性表明在处理此类病例时需要提高认识和警惕。
本病例报告强调,对于有皮肤SCC病史且出现新发腹部症状的患者,考虑小肠转移性疾病的重要性。