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间变性淋巴瘤激酶阴性的原发性系统性间变性大细胞淋巴瘤酷似头皮破裂的表皮囊肿:一例报告及文献复习

Anaplastic lymphoma kinase-negative primary systemic anaplastic large cell lymphoma mimicking a ruptured epidermal cyst of the scalp: a case report and literature review.

作者信息

Ahn Il Young, Bae Tae Hui, Kang Shin Hyuk, Woo Soo Hyun, Kim Woo Ju, Hong Min Eui, Kim Han Koo

机构信息

Department of Plastic and Reconstructive Surgery, Chung-Ang University Hospital, Seoul, Korea.

Department of Plastic and Reconstructive Surgery, Chung-Ang University Gwangmyeong Hospital, Gwangmyeong, Korea.

出版信息

Arch Craniofac Surg. 2024 Dec;25(6):298-302. doi: 10.7181/acfs.2024.00262. Epub 2024 Nov 18.

Abstract

The incidence of anaplastic large cell lymphoma is 0.25 cases per 100,000 people. It usually causes lymphadenopathy and B symptoms; however, diverse cutaneous manifestations can also be observed. We report a rare case of anaplastic large cell lymphoma of the scalp, which presented similarly to a ruptured epidermal cyst. A 77-year-old woman visited the outpatient clinic complaining of scalp masses that had appeared 2 months before. One week before her visit, she had undergone incision and drainage at a local clinic but showed no improvement. Before surgery, facial magnetic resonance imaging revealed two suspicious ruptured cystic masses. Surgical excision was performed with a 1-cm free margin from the soft mass. Histopathology confirmed anaplastic lymphoma kinase-negative anaplastic large cell lymphoma. After wide excision and skin grafting for wound reconstruction, followed by consultation with a hemato-oncologist and radiation oncologist, chemotherapy was planned to prevent recurrence. Differentiating anaplastic lymphoma kinase-negative anaplastic large cell lymphoma of the scalp from a ruptured epidermal cyst-like mass proved challenging. We recommend considering the possibility of anaplastic large cell lymphoma if an epidermal cyst-like mass does not respond to antibiotics or conventional dressing, as illustrated by our rare case.

摘要

间变性大细胞淋巴瘤的发病率为每10万人中有0.25例。它通常会导致淋巴结病和B症状;然而,也可观察到多种皮肤表现。我们报告一例罕见的头皮间变性大细胞淋巴瘤,其表现与破裂的表皮样囊肿相似。一名77岁女性因2个月前出现的头皮肿块到门诊就诊。就诊前一周,她在当地诊所接受了切开引流,但未见好转。手术前,面部磁共振成像显示两个可疑的破裂囊性肿块。对柔软肿块进行了1厘米切缘的手术切除。组织病理学证实为间变性淋巴瘤激酶阴性的间变性大细胞淋巴瘤。在进行广泛切除和皮肤移植以重建伤口后,经血液肿瘤学家和放射肿瘤学家会诊,计划进行化疗以预防复发。将头皮间变性淋巴瘤激酶阴性的间变性大细胞淋巴瘤与破裂的表皮样囊肿样肿块区分开来具有挑战性。正如我们这个罕见病例所示,如果表皮样囊肿样肿块对抗生素或传统敷料无反应,我们建议考虑间变性大细胞淋巴瘤的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a84d/11704716/566d28e01847/acfs-2024-00262f1.jpg

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