前额恶性肿瘤——两个病例报告及文献综述
Malignant Tumor of the Forehead—Two Cases Reports and a Literature Review
DOI: 10.12677/acm.2025.153751, PDF,   
作者: 张家豪:山东第一医科大学(山东省医学科学院)研究生部,山东 济南;刘广存*:山东第一医科大学第一附属医院神经外科,山东 济南
关键词: 额部罕见恶性肿瘤前额皮肤修补Frontal Rare Malignancy Frontal Skin Repair
摘要: 尽管大多数位于前额的肿瘤是良性的,但仍有恶性肿瘤发生,如果未能准确诊断并及时治疗可能导致不良预后。本报告详细描述了在一名51岁男性和一名72岁男性额头上发现的两例罕见恶性肿瘤。在第一例中,患者在右额部头皮上观察到肿块持续一年逐渐增大。磁共振成像(MRI)显示一个不均质性肿块,在T2-FLAIR加权和扩散加权成像(DWI)上表现为高信号,并在对比增强扫描中观察到明显增强。组织学分析显示细胞角蛋白(CK)阳性,CD56部分阳性,最终诊断为大细胞神经内分泌癌(LCNEC)。手术干预后,患者接受了放疗,在17个月的随访中,没有局部复发或远处转移的迹象。在第二例中,患者50年前在右额部发现一个肿块,肿块增大很少且未接受治疗。在心脏支架手术后,患者注意到三年前肿块迅速增大。计算机断层扫描(CT)显示信号均匀,未见颅骨侵犯。组织学检查显示CK7和上皮膜抗原(EMA)阳性,与汗腺癌一致,三个月的随访中没有局部复发或远处转移的迹象。我们对现有文献的回顾发现四例类似的罕见恶性肿瘤患者,这可能提供额外的诊断见解。此外,我们还研究了额头肿瘤切除后皮肤缺损的修补重建。
Abstract: Although most forehead tumors are benign, malignant tumors can also occur in this area. These tumors are highly aggressive and metastatic, and failure to diagnose and treat them appropriately can lead to a poor prognosis. Here, we describe two rare cases of malignant tumors occurring on the forehead in a 51-year-old man and a 72-year-old man. In the first case, the patient had a progressively enlarging mass on the right forehead for one year. Magnetic resonance imaging (MRI) revealed a heterogeneous mass with hyperintensity on T2-FLAIR and diffusion-weighted imaging (DWI). The mass showed distinct enhancement on contrast-enhanced scans. Histologically, the mass was positive for cytokeratin (CK) and partially positive for CD56. The patient was diagnosed with large cell neuroendocrine carcinoma (LCNEC). After surgical resection, the patient received radiotherapy. No local recurrence or distant metastasis was observed during the 17-month follow-up. In the second case, a mass was found on the right forehead 50 years ago. It had barely enlarged and was not treated. After undergoing heart stent surgery, the patient noticed rapid enlargement of the mass three years ago. Computed tomography (CT) showed a uniform signal without skull invasion. Histologically, the mass was positive for CK7 and epithelial membrane antigen (EMA), consistent with eccrine porocarcinoma. No local recurrence or distant metastasis was observed during the three-month follow-up. We reviewed the published literature and identified four previously reported cases of similar rare malignant tumors, which may provide additional diagnostic insights. We also explored the reconstruction of skin defects after forehead tumor resection.
文章引用:张家豪, 刘广存. 前额恶性肿瘤——两个病例报告及文献综述[J]. 临床医学进展, 2025, 15(3): 1366-1373. https://doi.org/10.12677/acm.2025.153751

参考文献

[1] Sgouros, D., Piana, S., Argenziano, G., Longo, C., Moscarella, E., Karaarslan, I.K., et al. (2013) Clinical, Dermoscopic and Histopathological Features of Eccrine Poroid Neoplasms. Dermatology, 227, 175-179. [Google Scholar] [CrossRef] [PubMed]
[2] Miyamoto, K., Yanagi, T., Maeda, T. and Ujiie, H. (2022) Diagnosis and Management of Porocarcinoma. Cancers, 14, 5232. [Google Scholar] [CrossRef] [PubMed]
[3] Salih, A.M., Kakamad, F.H., Baba, H.O., Salih, R.Q., Hawbash, M.R., Mohammed, S.H., et al. (2017) Porocarcinoma; Presentation and Management, a Meta-Analysis of 453 Cases. Annals of Medicine & Surgery, 20, 74-79. [Google Scholar] [CrossRef] [PubMed]
[4] Le, N., Janik, S., Liu, D.T., Grasl, S., Faisal, M., Pammer, J., et al. (2020) Eccrine Porocarcinoma of the Head and Neck: Meta‐analysis of 120 Cases. Head & Neck, 42, 2644-2659. [Google Scholar] [CrossRef] [PubMed]
[5] Belin, E., Ezzedine, K., Stanislas, S., Lalanne, N., Beylot-Barry, M., Taieb, A., et al. (2011) Factors in the Surgical Management of Primary Eccrine Porocarcinoma: Prognostic Histological Factors Can Guide the Surgical Procedure. British Journal of Dermatology, 165, 985-989. [Google Scholar] [CrossRef] [PubMed]
[6] Skowron, F., Poulhalon, N., Balme, B., Touzet, S. and Thomas, L. (2014) Étude clinique et histopronostique de 50 cas de porocarcinome eccrine. Annales de Dermatologie et de Vénéréologie, 141, 258-264. [Google Scholar] [CrossRef] [PubMed]
[7] Strosberg, J.R., Coppola, D., Klimstra, D.S., Phan, A.T., Kulke, M.H., Wiseman, G.A., et al. (2010) The NANETS Consensus Guidelines for the Diagnosis and Management of Poorly Differentiated (High-Grade) Extrapulmonary Neuroendocrine Carcinomas. Pancreas, 39, 799-800. [Google Scholar] [CrossRef] [PubMed]
[8] Burkeen, G., Chauhan, A., Agrawal, R., Raiker, R., Kolesar, J., Anthony, L., et al. (2020) Gynecologic Large Cell Neuroendocrine Carcinoma: A Review. Rare Tumors, 12, 1-11. [Google Scholar] [CrossRef] [PubMed]
[9] Korse, C.M., Taal, B.G., van Velthuysen, M.F. and Visser, O. (2013) Incidence and Survival of Neuroendocrine Tumours in the Netherlands According to Histological Grade: Experience of Two Decades of Cancer Registry. European Journal of Cancer, 49, 1975-1983. [Google Scholar] [CrossRef] [PubMed]
[10] Corbett, V., Arnold, S., Anthony, L. and Chauhan, A. (2021) Management of Large Cell Neuroendocrine Carcinoma. Frontiers in Oncology, 11, Article 653162. [Google Scholar] [CrossRef] [PubMed]
[11] Shin, M., Choi, C., Oh, Y. and Kim, N. (2011) CK20 Positive Large-Cell Neuroendocrine Carcinoma Presenting with Skin Metastases. Annals of Dermatology, 23, S20. [Google Scholar] [CrossRef] [PubMed]
[12] Almodovar-Real, A., Aneiros-Fernández, J. and Ruiz-Villaverde, R. (2016) A Slow-Growing Tumor on the Forehead. Actas Dermo-Sifiliográficas (English Edition), 107, 851-852. [Google Scholar] [CrossRef] [PubMed]
[13] Feng, Y. and Feng, J. (2023) A Giant Mass on the Forehead. BMJ, 380, p566. [Google Scholar] [CrossRef] [PubMed]
[14] Temelkova, I. and Tchernev, G. (2020) Tumorous Formation of the Forehead. Wiener Medizinische Wochenschrift, 170, 196-198. [Google Scholar] [CrossRef] [PubMed]
[15] Caldarelli, C., Autorino, U., Iaquinta, C. and De Marchi, A. (2019) Merkel Cell Carcinoma of the Forehead Area: A Literature Review and Case Report. Oral and Maxillofacial Surgery, 23, 365-373. [Google Scholar] [CrossRef] [PubMed]
[16] Folpe, A.L., Morris, R.J. and Weiss, S.W. (1999) Soft Tissue Giant Cell Tumor of Low Malignant Potential: A Proposal for the Reclassification of Malignant Giant Cell Tumor of Soft Parts. Modern Pathology, 12, 894-902.
[17] Rodríguez‐Peralto, J.L., Lopez‐Barea, F. and Fernandez‐Delgado, J. (2001) Primary Giant Cell Tumor of Soft Tissues Similar to Bone Giant Cell Tumor: A Case Report and Literature Review. Pathology International, 51, 60-63. [Google Scholar] [CrossRef] [PubMed]
[18] Cribier, B., Asch, P. and Grosshans, E. (1999) Differentiating Squamous Cell Carcinoma from Keratoacanthoma Using Histopathological Criteria. Dermatology, 199, 208-212. [Google Scholar] [CrossRef] [PubMed]
[19] Thandra, K.C., Barsouk, A., Saginala, K., Padala, S.A., Barsouk, A. and Rawla, P. (2021) Epidemiology of Non-Hodgkin’s Lymphoma. Medical Sciences, 9, Article 5. [Google Scholar] [CrossRef] [PubMed]
[20] Gao, Y., Huang, H.H., Lin, X.B., Cai, Q.Q., Pan, Z.H., Wang, B.F. and Bu, Q. (2007) Treatment Outcomes and Prognostic Analyses of Relapsed or Refractory T-Cell Non-Hodgkin’s Lymphoma. Chinese Journal of Cancer, 26, 909-913.
[21] Heath, M., Jaimes, N., Lemos, B., Mostaghimi, A., Wang, L.C., Peñas, P.F., et al. (2008) Clinical Characteristics of Merkel Cell Carcinoma at Diagnosis in 195 Patients: The AEIOU Features. Journal of the American Academy of Dermatology, 58, 375-381. [Google Scholar] [CrossRef] [PubMed]
[22] Neumann, C.G. (1957) The Expansion of an Area of Skin by Progressive Distention of a Subcutaneous Balloon. Plastic and Reconstructive Surgery, 19, 124-130. [Google Scholar] [CrossRef] [PubMed]
[23] Bradford, B.D. and Lee, J.W. (2019) Reconstruction of the Forehead and Scalp. Facial Plastic Surgery Clinics of North America, 27, 85-94. [Google Scholar] [CrossRef] [PubMed]
[24] Hwang, L., Ford, N., Spitz, J. and Ellis, M. (2017) The Visor Flap. Journal of Craniofacial Surgery, 28, e146-e148. [Google Scholar] [CrossRef] [PubMed]