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Lupus Erythematosus Tumidus Misdiagnosed as Erythema Nodosum from Coccidioidomycosis. 红斑狼疮瘤被误诊为球孢子菌病结节性红斑
IF 0.9 Q4 DERMATOLOGY Pub Date : 2024-05-23 eCollection Date: 2024-01-01 DOI: 10.1159/000538737
Brianae Garcia, Anis Hasnaoui, Prakash V A K Ramdass

Introduction: Lupus erythematosus tumidus (LET) is a rare photosensitive dermatosis that is categorized as intermittent cutaneous lupus erythematosus. It shares clinical similarities and histopathological features with other skin disorders, such as erythema nodosum, lymphocytic infiltrate of Jessner, and reticular erythematous mucinosis, thus making diagnosis quite challenging. We present a patient with LET whose diagnosis was confirmed after seeing several doctors.

Case presentation: A 52-year-old Hispanic female presented with tender erythematous nodules on her thighs for approximately 1 month. She was suspected of having erythema nodosum secondary to coccidioidomycosis and was prescribed fluconazole 200 mg for 30 days but showed no improvement. However, histopathological and direct immunofluorescence tests later confirmed a diagnosis of LET. The patient was treated with hydroxychloroquine, and the lesions improved remarkably after 2 weeks.

Conclusion: LET is a rare dermatosis that closely resembles other dermatologic conditions such as erythema nodosum, lymphocytic infiltrate of Jessner, and reticular erythematous mucinosis. Diagnosis based on clinical features alone should be avoided, and ideally, treatment should only be initiated after confirmatory histopathological testing.

简介肿瘤性红斑狼疮(LET)是一种罕见的光敏性皮肤病,被归类为间歇性皮肤红斑狼疮。它与结节性红斑、杰斯纳淋巴细胞浸润、网状红斑性粘液病等其他皮肤病有相似的临床和组织病理学特征,因此诊断颇具挑战性。我们为大家介绍一位 LET 患者,她在看了几位医生后才被确诊:一名 52 岁的西班牙裔女性,大腿上出现触痛性红斑结节约 1 个月。她被怀疑是继发于球孢子菌病的结节性红斑,医生给她开了氟康唑 200 毫克,连用 30 天,但没有好转。然而,后来的组织病理学和直接免疫荧光检测证实了 LET 的诊断。患者接受了羟氯喹治疗,2 周后皮损明显好转:结论:LET 是一种罕见的皮肤病,与结节性红斑、杰斯纳淋巴细胞浸润和网状红斑粘液病等其他皮肤病非常相似。应避免仅根据临床特征进行诊断,最好在组织病理学检测确诊后再开始治疗。
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引用次数: 0
Characteristic Skin Eruptions with a Distinct Histological Pattern Allow Early Diagnosis of Vitamin C Deficiency. 具有独特组织学模式的特征性皮肤溃疡可用于维生素 C 缺乏症的早期诊断。
IF 0.9 Q4 DERMATOLOGY Pub Date : 2024-05-21 eCollection Date: 2024-01-01 DOI: 10.1159/000538916
Goran Mirkovic, Markus Reinhold Mutke, Beda Muehleisen

Introduction: Scurvy has become a rare disease in western countries with potentially high morbidity. Early diagnosis is crucial and can be challenging.

Case presentation: We present the case of a 56-year-old male patient who developed hemorrhagic diathesis after trivial impact trauma. Previously, the patient suffered from fatigue and loss of appetite. Characteristic skin eruptions and a distinct skin histology along with a decreased serum vitamin C level led to the diagnosis of scurvy. Following vitamin C supplementation, symptoms improved rapidly.

Conclusion: In conclusion, vitamin C deficiency should be considered in cases with unclear hemorrhagic diathesis and a medical history of nutritional irregularities. Especially in cases of scurvy that do not yet show the full clinical spectrum of symptoms or have only moderately decreased serum vitamin C levels, thorough clinical dermatological examination and a skin biopsy are essential for early diagnosis and to prevent complications.

导言:坏血病在西方国家已成为一种罕见疾病,发病率可能很高。早期诊断至关重要,但也很有难度:本病例是一名 56 岁的男性患者,因轻微撞击外伤导致出血性休克。在此之前,患者经常感到疲倦和食欲不振。患者皮肤出现特征性糜烂,皮肤组织学特征明显,血清维生素 C 水平下降,因此被诊断为坏血病。补充维生素 C 后,症状迅速得到改善:总之,对于出血症状不明确、有营养失调病史的病例,应考虑维生素 C 缺乏症。特别是对于临床症状不明显或血清维生素 C 水平中度下降的坏血病病例,彻底的临床皮肤病检查和皮肤活检对于早期诊断和预防并发症至关重要。
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引用次数: 0
Pityriasis Lichenoides et Varioliformis Acuta Developing during Pembrolizumab Treatment for Bladder Cancer. 彭博利珠单抗(Pembrolizumab)治疗膀胱癌期间出现的脓疱疮和苔藓样变。
IF 0.9 Q4 DERMATOLOGY Pub Date : 2024-05-17 eCollection Date: 2024-01-01 DOI: 10.1159/000538767
Yuki Mizutani, Ena Noda, Makoto Kondo, Akinobu Hayashi, Keiichi Yamanaka

Introduction: Anti-PD-1 immunotherapies enhance T-cell responses against tumor cells by blocking the interaction between PD-1 and its ligand, PD-L1. While these therapies offer significant benefits in treating various malignancies, they can also lead to several immune-related adverse events (irAEs), most notably manifesting in the skin. Lichenoid reactions, eczema, and vitiligo are the three most prevalent forms of cutaneous irAE.

Case presentation: Here, we report a rare case of a pityriasis lichenoides et varioliformis acuta (PLEVA) that developed during pembrolizumab treatment for invasive bladder cancer. A 53-year-old man, receiving pembrolizumab for invasive bladder cancer, developed erythematous papules on his legs after his 11th infusion. The skin lesions gradually spread to his entire trunk and extremities. A punch biopsy revealed several apoptotic keratinocytes and spongiosis, along with perivascular and lichenoid lymphocytic infiltration with vacuolar alteration. Immunohistochemistry showed infiltration of CD4+ and CD8+ T cells in both the epidermis and dermis. Granzyme B-positive inflammatory cells were also slightly present. From these results, he was diagnosed with PLEVA, which might be classified as a lichenoid eruption, especially based on the histological findings.

Conclusion: We hypothesize that the anti-PD-1 antibody might lead to epidermal necrosis by amplifying the expression of cytolytic molecules such as granzyme B in CD8+ T cells.

简介抗PD-1免疫疗法通过阻断PD-1与其配体PD-L1之间的相互作用,增强T细胞对肿瘤细胞的反应。虽然这些疗法在治疗各种恶性肿瘤方面有显著疗效,但也会导致一些免疫相关不良反应(irAEs),最明显的是皮肤不良反应。苔癣样反应、湿疹和白癜风是三种最常见的皮肤irAE:在此,我们报告了一例罕见的在治疗侵袭性膀胱癌的 Pembrolizumab 过程中出现的类苔藓反应(PLEVA)。一名 53 岁的男子正在接受 pembrolizumab 治疗浸润性膀胱癌,在第 11 次输液后,他的腿部出现了红斑丘疹。皮损逐渐扩散到整个躯干和四肢。穿刺活检显示,有多个角朊细胞凋亡和海绵状增生,血管周围和苔藓样淋巴细胞浸润,并伴有空泡改变。免疫组化显示,表皮和真皮均有 CD4+ 和 CD8+ T 细胞浸润。Granzyme B 阳性的炎症细胞也略有存在。根据这些结果,他被诊断为 PLEVA,尤其是根据组织学结果,这可能被归类为苔癣样糜烂:我们推测,抗 PD-1 抗体可能会通过扩大 CD8+ T 细胞中颗粒酶 B 等细胞溶解分子的表达而导致表皮坏死。
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引用次数: 0
Successful Removal of 17 Tattoos Self-Administered Using Black Eyeliner Ink with Quality-Switched Neodymium-Doped Yttrium Aluminum Garnet 1,064-nm Laser: A Case Report 使用质量开关掺钕钇铝石榴石 1,064 nm 激光成功去除 17 个使用黑色眼线墨水自制的纹身:病例报告
IF 0.9 Q3 Medicine Pub Date : 2024-04-22 DOI: 10.1159/000538555
S. M. S. Jafari, Simon Bossart, Maurice A. Adatto, Laurence Feldmeyer, Nikhil Yawalkar, K. Heidemeyer
Abstract Introduction Tattooing has a rich historical presence in various human civilizations, with the earliest physical evidence dating back to around 3258 BC. While acceptance of tattoos is increasing in the Western world, negative associations remain. Short-pulsed lasers, such as Q-Switched (QS) or picosecond lasers, are the gold standard for tattoo removal. Case Presentation This case report discusses the successful removal of 17 amateur tattoos, which were self-administered by a 19-year-old female patient using black eyeliner ink and sewing needles. The tattoos, distributed across her body, including the face and hands, were partially or completely removed over 10 sessions using the QS Neodymium-doped Yttrium Aluminum Garnet 1,064-nm laser. Conclusion The factors that influence the efficacy of tattoo removal are highlighted, including tattoo type, location, and coexisting fibrosis. The psychological and social importance of effective tattoo removal is emphasized, particularly for young people seeking to disassociate from past experiences or affiliations.
摘要 导言 纹身在各种人类文明中都有着丰富的历史,最早的实物证据可追溯到公元前 3258 年左右。虽然西方世界对纹身的接受度越来越高,但负面的联想依然存在。短脉冲激光,如 Q-Switched (QS) 或皮秒激光,是去除纹身的黄金标准。病例介绍 本病例报告讨论了一名 19 岁女性患者使用黑色眼线墨水和缝衣针成功去除 17 个业余纹身的案例。这些纹身分布在她的全身,包括脸部和手部,使用 QS 掺钕钇铝石榴石 1,064 纳米激光,经过 10 次治疗,部分或全部去除。结论 强调了影响纹身去除效果的因素,包括纹身类型、位置和并存的纤维化。强调了有效去除纹身在心理和社会方面的重要性,尤其是对于那些希望与过去的经历或隶属关系脱离关系的年轻人。
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引用次数: 0
Thoracocervicofacial Purpura as a Presenting Symptom of Seizure Disorder: A Case Report 胸颈面部紫癜是癫痫发作的先兆症状:病例报告
IF 0.9 Q3 Medicine Pub Date : 2024-04-10 DOI: 10.1159/000537901
Waseem K. Alhawsawi, K. A. Hawsawi, Alhusain Alshareef, Rama Halabi, Ammar Baksh, Basant A Alzubaidy
Abstract Introduction Postictal thoracocervicofacial purpura (PTP) is a rare clinical sign after a seizure episode and may be the only objective sign seen in patients who are unaware of their own seizure disorder. Moreover, it can be the only reason a patient seeks medical care after a seizure activity. Case Presentation Herein, we report a 23-year-old, living alone and not known to have any medical illnesses, who presented to our emergency department complaining of asymptomatic purpuric facial rash extending to his neck and upper chest that started suddenly when he woke up that morning. Tongue and distal lateral thigh erosions were also noticed during physical examination, as well as conjunctival hemorrhage. In addition, the patient stated that he experienced similar prior episode of purpuric rash over the face, and disappeared uneventfully within 2 weeks. Blood work was remarkable for elevated urine creatinine (21,692 mg/L) and creatine kinase (1,207 mg/L). Given his clinical features and initial laboratory results, a diagnosis of PTP was made. Conclusion Patients who present with petechial rash over the chest, neck, malar area along with conjunctival hemorrhage as an only complaint should be suspected to have or evaluated for seizure disorder.
摘要 引言 发作后胸颈面部紫癜(PTP)是癫痫发作后的一种罕见临床表现,可能是不知道自己患有癫痫发作疾病的患者所看到的唯一客观体征。此外,它还可能是患者在癫痫发作后就医的唯一原因。病例介绍 在此,我们报告了一名 23 岁的独居患者,据悉他没有任何内科疾病,来我院急诊科就诊时主诉其面部出现无症状紫癜性皮疹,皮疹延伸至颈部和上胸部,于当天早晨醒来时突然开始。体检时还发现舌头和大腿远外侧糜烂,以及结膜出血。此外,患者还表示,他之前也曾出现过类似的面部紫癜性皮疹,但在两周内顺利消失。血液检查结果显示尿肌酐(21692 毫克/升)和肌酸激酶(1207 毫克/升)升高。鉴于他的临床特征和最初的实验室结果,诊断为 PTP。结论 如果患者仅以胸部、颈部和颊部出现瘀斑皮疹和结膜出血为主诉,则应怀疑或评估是否患有癫痫发作疾病。
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引用次数: 0
Efficacy of Siltuximab and 1,927 nm Fractional Laser for the Treatment of Cutaneous Manifestations in Castleman’s Disease: The Role of Dermoscopy and Reflectance Confocal Microscopy for Lesion Evaluation 西妥昔单抗和1,927 nm点阵激光治疗卡斯特曼病皮肤症状的疗效:皮肤镜和反射共聚焦显微镜在病变评估中的作用
IF 0.9 Q3 Medicine Pub Date : 2024-04-08 DOI: 10.1159/000536483
G. Paolino, Marco Ardigò, E. Della-Torre, Luca Moroni, N. Rizzo, Matteo Riccardo Di Nicola, V. G. Bianchi, Lorenzo Dagna, Giuseppe Alvise Ramirez, S. Mercuri
Abstract Introduction Multicentric Castleman’s disease (MCD) with cutaneous involvement has rarely been discussed in dermatologic literature, with few reports. Cutaneous lesions in MCD may induce deep scars, causing a significant impact in the daily life of the patients. The treatment of Castleman’s disease (CD) is usually a challenge, especially in case of cutaneous involvement. Case Presentation We report the case of a 35-year-old Caucasian man with a 3-year-old history of MCD with cutaneous involvement that we treated with a combined therapy characterized by siltuximab and 1,927 nm fractional laser. The patient showed a therapeutic response, characterized by a reduction of systemic symptoms and cutaneous manifestations. Conclusion We believe that the combination of siltuximab and 1,927 nm fractional laser might have a synergistic beneficial role in patients with cutaneous iMCD and maximize esthetic outcomes. Anyway, additional evidence is needed to validate our findings.
摘要 引言 多中心卡斯特曼病(MCD)伴有皮肤受累,在皮肤科文献中鲜有报道。多中心卡斯特曼病(MCD)的皮肤病变可诱发深度疤痕,对患者的日常生活造成严重影响。卡斯特曼病(CD)的治疗通常是一项挑战,尤其是在皮肤受累的情况下。病例介绍 我们报告了一例 35 岁的白种男性病例,他有 3 年的 MCD 病史,并伴有皮肤受累,我们采用了以西妥昔单抗和 1927 纳米点阵激光为特征的联合疗法进行治疗。患者出现了治疗反应,全身症状和皮肤表现均有所减轻。结论 我们认为,联合使用西妥昔单抗和 1927 纳米点阵激光可能会对皮肤 iMCD 患者起到协同增效的作用,并最大限度地提高美容效果。无论如何,还需要更多的证据来验证我们的研究结果。
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引用次数: 0
The Cystic Sponge Anus 海绵囊肿肛门
IF 0.9 Q3 Medicine Pub Date : 2024-04-02 DOI: 10.1159/000536085
H. H. van der Zee, P. Aarts
Abstract Introduction A peculiar spongy appearance of the perianal skin was observed in a patient who underwent wide excision surgery for inguinal and gluteal hidradenitis suppurativa (HS). Case Presentation This peculiar appearance was observed in a 62-year-old male patient. It included multiple orifices and cavities forming the spongy aspect of the perianal skin with multiple cysts and giant comedones. The perianal lesions were asymptomatic and the patient had never received any perianal treatment for the comedones or cysts. Histopathology was performed and demonstrated dilated hair follicles with flaky keratin and loose hair shafts in the center. The spongy appearance was most likely the result of spontaneous shedding of the cystic contents. Conclusion We suspect that the “cystic sponge anus” might be associated with HS, smoking, the male gender, and may yet be another expression of an occlusive follicular disease. Future studies will be needed to clarify the prevalence and comorbidities of the “cystic sponge anus.”
摘要 引言 一名因腹股沟和臀部化脓性扁平苔癣(HS)而接受广泛切除手术的患者,其肛周皮肤出现了奇特的海绵状外观。病例介绍 在一名 62 岁的男性患者身上观察到了这种奇特的外观。患者的肛周皮肤呈海绵状,并伴有多个囊肿和巨大粉刺,其中包括多个孔和空腔。肛周病变无症状,患者从未因粉刺或囊肿接受过任何肛周治疗。组织病理学检查显示,患者的毛囊扩张,角质脱落,中心的毛干松散。海绵状外观很可能是囊肿内容物自发脱落的结果。结论 我们怀疑 "海绵囊肿性肛门 "可能与 HS、吸烟和男性有关,也可能是闭塞性毛囊疾病的另一种表现形式。未来的研究需要明确 "海绵囊肿性肛门 "的发病率和合并症。
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引用次数: 0
Expanding the Differential Diagnosis of the Painful Nail: A Case of an Onychopapilloma with Neuroma. 扩展疼痛性指甲的鉴别诊断:一例伴有神经瘤的趾甲瘤
IF 0.9 Q3 Medicine Pub Date : 2024-03-28 eCollection Date: 2024-01-01 DOI: 10.1159/000538087
Jade Conway, Cynthia M Magro, Shari R Lipner

Introduction: Onychopapilloma most commonly presents as longitudinal erythronychia, but diagnosis may be challenging in some cases due to varied clinical presentations. Most patients with onychopapillomas do not report associated pain but instead more commonly report functional interference.

Case report: We present a case of a 74-year-old female with a 5-year history of splitting and lifting of the right thumbnail, accompanied by nail sensitivity and intermittent painful throbbing. Clinical examination was significant for a less than 1 mm red line with distal onycholysis. Love's test and a cold test performed with ice pack were negative. X-ray of the right thumb was negative for erosion or exostosis. Nail biopsy was performed, and dermatopathology was consistent with onychopapilloma with a concomitant traumatic neuroma.

Conclusion: We report a case of onychopapilloma with a concomitant traumatic neuroma. Subungual neuromas are extremely rare and have not previously been associated with onychopapilloma. Our case supports the expansion of the differential diagnosis for a painful nail and demonstrates the importance of diagnostic confirmation with biopsy and histopathology.

导言:网状乳头状瘤最常见的表现是纵向红斑,但由于临床表现各异,有些病例的诊断可能具有挑战性。大多数网状乳头状瘤患者并不伴有疼痛,而更多地表现为功能障碍:我们报告了一例 74 岁女性患者的病例,她的右手拇指指甲有 5 年的劈裂和翘起病史,并伴有指甲敏感和间歇性刺痛。临床检查结果表明,其远端甲沟炎红线不到 1 毫米。爱氏试验和用冰袋进行的冷试验均为阴性。右手拇指的 X 射线检查未发现糜烂或骨质增生。进行了指甲活组织检查,皮肤病理学检查结果与甲状软骨瘤一致,同时伴有创伤性神经瘤:我们报告了一例甲上皮脂瘤并发外伤性神经瘤的病例。舌下神经瘤极为罕见,以前从未与甲状软骨瘤联系在一起。我们的病例支持扩大指甲疼痛的鉴别诊断范围,并证明了活检和组织病理学确诊的重要性。
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引用次数: 0
Diffuse Lichen Planopilaris Masquerading as Diffuse Alopecia Areata. 伪装成弥漫性脱发的弥漫性扁平苔癣
IF 0.9 Q3 Medicine Pub Date : 2024-03-25 eCollection Date: 2024-01-01 DOI: 10.1159/000538064
Li Jie Helena Yoo, Nekma Meah, Dmitri Wall, Ian McDonald

Introduction: Lichen planopilaris (LPP) is a primary lymphocytic cicatricial alopecia that represents a form of follicular lichen planus.

Case presentation: We describe a case of coexisting diffuse LPP and female pattern hair loss masquerading as diffuse alopecia areata in a 32-year-old female.

Discussion: In complex cases such as this, dermoscopy-guided vertical and horizontal biopsies from androgen sensitive and insensitive areas are helpful in increasing diagnostic yield. Prompt initiation of treatment is key to halting disease progression. Long-term follow-up is important as resolution of clinical signs does not always correlate with the absence of disease progression.

导言:扁平苔藓(LPP)是一种原发性淋巴细胞环状脱发,是毛囊性扁平苔藓的一种表现形式:我们描述了一例 32 岁女性同时患有弥漫性扁平苔藓和伪装成弥漫性脱发的女性型脱发病例:对于此类复杂病例,在皮肤镜引导下从雄激素敏感和不敏感区域进行垂直和水平活检有助于提高诊断率。及时开始治疗是阻止疾病进展的关键。长期随访非常重要,因为临床症状的缓解并不总是与疾病无进展相关联。
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引用次数: 0
Management of Locally Advanced Basal Cell Carcinoma with Sonic Hedgehog Pathway Targeted Therapy: A Case Report and Discussion. 用音速刺猬蛋白通路靶向疗法治疗局部晚期基底细胞癌:病例报告与讨论
IF 0.9 Q3 Medicine Pub Date : 2024-03-13 eCollection Date: 2024-01-01 DOI: 10.1159/000537817
Neal Ferrin, Darwin Edmond, Ryan Jones, Laurence E McCahill

Introduction: Basal cell carcinoma (BCC) is the most common skin malignancy in the world. While most lesions are treated using surgical methods, others may present as locally advanced or metastatic disease and are not amenable to surgical therapy alone. Treatment with sonic hedgehog pathway inhibitors (vismodegib, sonidegib) is designed to inhibit key signaling proteins and gene pathways involved with BCC to reduce the uncontrolled proliferation of basal cells in complicated disease and can be invaluable in treating patients with advanced disease.

Case presentation: We describe the course of a 68-year-old man who presented with a 7.2 × 6 cm exophytic and ulcerated locally invasive BCC of his upper back. The patient was started on daily vismodegib treatment with the goal of eventual surgical resection. After 11 weeks of therapy, he had significant improvement in both wound size and appearance. After 18 weeks of therapy, he had achieved a near complete clinical response of the central aspect of lesion with three remaining small peripheral lesions. These lesions were biopsied, and two were found to be negative for malignancy, while a small inferior nodule was positive for squamous cell carcinoma (SCC). Vismodegib therapy was discontinued after a total of 26 weeks of therapy. Excision of the SCC was performed, and the patient remains disease free at 2 years.

Conclusion: This case report shows the efficacy of hedgehog pathway inhibitor therapy in the treatment of a locally advanced BCC with complete pathologic response, not requiring surgical intervention.

简介:基底细胞癌(BCC)是世界上最常见的皮肤恶性肿瘤:基底细胞癌(BCC)是世界上最常见的皮肤恶性肿瘤。虽然大多数病变可通过外科手术治疗,但也有一些病变可能是局部晚期或转移性疾病,无法仅通过外科手术治疗。使用声刺猬通路抑制剂(vismodegib、sonidegib)治疗的目的是抑制与 BCC 相关的关键信号蛋白和基因通路,以减少复杂疾病中基底细胞不受控制的增殖,对于治疗晚期患者非常有价值:我们描述了一名 68 岁男性患者的病程,他的上背部有一个 7.2 × 6 厘米的外生溃疡性局部浸润性 BCC。患者开始接受每日 vismodegib 治疗,目标是最终进行手术切除。治疗 11 周后,他的伤口大小和外观都有了明显改善。治疗 18 周后,他的病变中央部位几乎达到了完全临床反应,但周边仍有三个小病灶。对这些病灶进行了活组织检查,发现其中两个病灶的恶性程度为阴性,而下部的一个小结节则为鳞状细胞癌(SCC)阳性。Vismodegib 治疗共 26 周后停止。患者接受了 SCC 切除术,2 年后仍未患病:本病例报告显示了刺猬通路抑制剂治疗局部晚期 BCC 的疗效,病理反应完全,无需手术干预。
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引用次数: 0
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Case Reports in Dermatology
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