今日の臨床サポート 今日の臨床サポート

著者: 清原隆宏 関西医科大学 総合医療センター皮膚科

監修: 戸倉新樹 掛川市・袋井市病院企業団立 中東遠総合医療センター 参与/浜松医科大学 名誉教授

著者校正/監修レビュー済:2022/06/23
参考ガイドライン:
  1. 日本皮膚科学会:皮膚悪性腫瘍ガイドライン第3版 有棘細胞癌診療ガイドライン2020
患者向け説明資料

改訂のポイント:
  1. 有棘細胞癌診療ガイドライン2020に基づいた切除マージンを記載した。

概要・推奨   

  1. 高齢者に生じる単発性の扁平隆起性局面をみたら、ボーエン病を想起する。
 

病態・疫学・診察 

疾患情報(疫学・病態)  
  1. 病因の特定できない表皮内癌を一般にボーエン病という。
  1. 1912年に前癌病変として初めて報告されたが[1]、現在では表皮ケラチノサイトの癌そのものと考えられている。
  1. 亀頭部のボーエン病は紅色肥厚症と呼ばれ、ボーエン病に先んじて1911年に報告された[2]
  1. 60歳以上の高齢者に多く、男女比はほぼ同等である。
  1. 全身皮膚のどこにでも発生し、体幹や四肢に多いが、爪床や爪母に生じることがある。
  1. 露光部では日光、非露光部では砒素の関与が示唆されているが、日光や砒素の関与が明らかな場合はそれぞれボーエン様型日光角化症、砒素角化症・砒素癌などと診断される。
  1. ヒト乳頭腫ウイルス(human papillomavirus、HPV)の関与を示唆する多くの報告がされており、HPV16、18、31、33、34、53、54、58、61、62、73型などのさまざまなタイプが検出されている[3][4][5]
  1. 疣贅状表皮発育異常症の病変内に生じる場合はHPV3、5、8、10型などの関与がある[6][7]
  1. 爪や指のボーエン病では、HPV16、56が検出されることがある。
問診・診察のポイント  
  1. 通常は単発性である。

これより先の閲覧には個人契約のトライアルまたはお申込みが必要です。

最新のエビデンスに基づいた二次文献データベース「今日の臨床サポート」。
常時アップデートされており、最新のエビデンスを各分野のエキスパートが豊富な図表や処方・検査例を交えて分かりやすく解説。日常臨床で遭遇するほぼ全ての症状・疾患から薬剤・検査情報まで瞬時に検索可能です。

まずは15日間無料トライアル
本サイトの知的財産権は全てエルゼビアまたはコンテンツのライセンサーに帰属します。私的利用及び別途規定されている場合を除き、本サイトの利用はいかなる許諾を与えるものでもありません。 本サイト、そのコンテンツ、製品およびサービスのご利用は、お客様ご自身の責任において行ってください。本サイトの利用に基づくいかなる損害についても、エルゼビアは一切の責任及び賠償義務を負いません。 また、本サイトの利用を以て、本サイト利用者は、本サイトの利用に基づき第三者に生じるいかなる損害についても、エルゼビアを免責することに合意したことになります。  本サイトを利用される医学・医療提供者は、独自の臨床的判断を行使するべきです。本サイト利用者の判断においてリスクを正当なものとして受け入れる用意がない限り、コンテンツにおいて提案されている検査または処置がなされるべきではありません。 医学の急速な進歩に鑑み、エルゼビアは、本サイト利用者が診断方法および投与量について、独自に検証を行うことを推奨いたします。

文献 

J T Bowen
Centennial paper. May 1912 (J Cutan Dis Syph 1912;30:241-255). Precancerous dermatoses: a study of two cases of chronic atypical epithelial proliferation. By John T. Bowen, M.D., Boston.
Arch Dermatol. 1983 Mar;119(3):243-60.
Abstract/Text
PMID 6297414
Queyrat L: Erythroplasia du gland. Paris: Bull Soc Franc de dermat et syph, 1911; 22: 378-382.
H Ikenberg, L Gissmann, G Gross, E I Grussendorf-Conen, H zur Hausen
Human papillomavirus type-16-related DNA in genital Bowen's disease and in Bowenoid papulosis.
Int J Cancer. 1983 Nov 15;32(5):563-5.
Abstract/Text 32P-labelled DNA of HPV 16 which has been isolated and molecularly cloned from a cervical carcinoma (Dürst et al., 1983) was used to screen the cellular DNAs obtained from 20 different biopsies of Morbus Bowen or Bowenoid papulosis, respectively, by Southern blot analysis. Under conditions of differing stringency for the hybridization, HPV 16 DNA or related sequences were identified in 6 out of 10 cases of Morbus Bowen (4 out of 5 from a genital localization) and in 8 out of 10 biopsies from Bowenoid papulosis. One additional case of the latter disease contained DNA sequences of an HPV type not yet classified. There is evidence for the presence of another HPV DNA in two of the HPV-16-positive tumors. A large number of normal genital tissue samples were negative for HPV DNA.

PMID 6315601
T Mitsuishi, T Sata, T Matsukura, T Iwasaki, M Kawashima
The presence of mucosal human papillomavirus in Bowen's disease of the hands.
Cancer. 1997 May 15;79(10):1911-7.
Abstract/Text BACKGROUND: Bowen's disease (BD) of the genital skin region is generally associated with human papillomavirus (HPV) infection. Various molecular analyses have identified mainly HPV-16 in the lesions. However, the HPV genotypes associated with BD of the hands have not yet been characterized.
METHODS: The skin specimens of 12 patients with BD of the hands were investigated clinicopathologically and immunohistochemically, and the total DNAs extracted from the skin were analyzed for the presence of HPV DNA using Southern blot hybridization and polymerase chain reaction (PCR) in combination with restriction fragment length polymorphisms (RFLP) and direct sequencing analysis of the amplified products. In addition, the histologic localization of HPV DNA was examined by in situ hybridization in paraffin embedded sections of HPV positive patients.
RESULTS: In 8 of 12 BD lesions (66.7%), HPV types (HPV-16, -31, -54, -58, -61, -62, and -73) were detected by Southern blot hybridization and/or PCR with RFLP and direct sequencing analysis. In 6 of 7 HPV positive lesions examined (85.7%), the viral genomes were identified by in situ hybridization in the nuclei of keratinocytes in the upper stratum malpighii and/or stratum corneum.
CONCLUSIONS: These results demonstrate that BD of the hands is frequently associated with HPV infection. The seven HPV genotypes are known as mucosal (genital) HPVs and to the authors' knowledge, this is the first time HPV-31, -54, -58, -61, -62, and -73 have been identified in BD lesions. These findings strongly suggest that HPVs related to mucosal lesions play an important role in the development of BD of the hands.

PMID 9149017
三石 剛ほか: Bowen病とヒト乳頭腫ウイルス. 臨床皮膚科1998; 52: 65-70.
L M Tieben, R J Berkhout, H L Smits, J N Bouwes Bavinck, B J Vermeer, J A Bruijn, F J Van der Woude, J Ter Schegget
Detection of epidermodysplasia verruciformis-like human papillomavirus types in malignant and premalignant skin lesions of renal transplant recipients.
Br J Dermatol. 1994 Aug;131(2):226-30.
Abstract/Text To evaluate the putative role of human papillomaviruses (HPV) in the development of skin cancer in renal transplant recipients, a series of skin biopsies from premalignant and malignant skin lesions was analysed using the polymerase chain reaction. Four different consensus primer pairs were used. HPV DNA was detected in five of 24 cases of squamous cell carcinoma, in one of three cases of Bowen's disease, in none of four basal cell carcinomas, in two of seven cases of actinic keratosis and in one of five cases of keratoacanthoma. Typing by direct sequencing of the amplified HPV DNA was possible in seven of nine cases, and revealed epidermodysplasia verruciformis (EV)-associated HPV types, or HPV types related to EV-associated types. Hence, HPV DNA could be detected in a significant proportion of (pre)malignant skin tumours in renal transplant recipients. The finding that some of the detected HPV types were as yet uncharacterized EV-related types, suggests that HPV DNA could be present in a higher percentage of lesions, and might be detected with refinement of the techniques.

PMID 7917987
T G Berger, W S Sawchuk, C Leonardi, A Langenberg, J Tappero, P E Leboit
Epidermodysplasia verruciformis-associated papillomavirus infection complicating human immunodeficiency virus disease.
Br J Dermatol. 1991 Jan;124(1):79-83.
Abstract/Text Three males infected with the human immunodeficiency virus (HIV) were noted to have extensive flat warts of the face and/or body. In two there were also pityriasis versicolor-like lesions. Biopsies showed foamy, basophilic, distended cytoplasm in granular layer keratinocytes, characteristic of the human papillomavirus types seen in epidermodysplasia verruciformis. DNA hybridization techniques demonstrated the presence of HPV-type 8 in one patient and HPV 5 and 8 in another. Patients with immune suppression due to HIV infection may demonstrate the clinical features of epidermodysplasia verruciformis with the same potentially oncogenic HPV types.

PMID 1847068
高田 実: Bowen病, 診断と治療指針. Skin Cancer1994; 9: 27-28.
安齋眞一ほか: 皮膚悪性腫瘍ガイドライン第3版 有棘細胞癌診療ガイドライン2020. 日皮会誌2020; 130: 2501-2533.
Schwartz RA et al: Bowen’s disease, In: Fitzpatrick’s Dermatology in general medicine, 5th ed, New York:McGraw-Hill, 1999; 832-834.
布袋祐子ほか: エトレチネート内服にて軽快傾向を認めた多発性ボーエン病の1例. 臨床皮膚科1997; 51: 951-953.
C A Morton, C Whitehurst, J H McColl, J V Moore, R M MacKie
Photodynamic therapy for large or multiple patches of Bowen disease and basal cell carcinoma.
Arch Dermatol. 2001 Mar;137(3):319-24.
Abstract/Text BACKGROUND: Photodynamic therapy (PDT) using topical delta-aminolevulinic acid (delta-ALA) is an effective treatment for Bowen disease and certain basal cell carcinomas (BCCs), but its place in clinical practice remains to be established. Patients with large and/or multiple lesions of Bowen disease or BCC can represent a considerable therapeutic challenge. We suggest that delta-ALA PDT may be of particular benefit in such patients.
OBSERVATION: In an open study, 35 (88%) of 40 large patches of Bowen disease, all with a maximum diameter greater than 20 mm, cleared following 1 to 3 treatments of delta-ALA PDT, although 4 patches recurred within 12 months. delta-Aminolevulinic acid PDT was also used to treat 40 large BCCs, with an identical 88% initial clearance (after 1-3 treatments), with 4 recurrences within 34 months (range, 12-60 months). In 10 further patients with multiple (> or =3) patches of Bowen disease, 44 (98%) of 45 patches cleared following delta-ALA PDT, although 4 lesions recurred over 12 months. In 3 patients with multiple BCCs, PDT cleared 52 (90%) of 58 lesions, with 2 recurrences during 41 months (range, 12-52 months). Treatments were well tolerated, with only 5 patients with solitary large lesions requiring local anesthesia.
CONCLUSIONS: delta-Aminolevulinic acid PDT is an effective tissue-sparing modality achieving good cosmesis. We propose that delta-ALA PDT be considered as a first-line therapy for large and/or multiple areas of Bowen disease and superficial BCCs.

PMID 11255332
M Hiruma, A Kawada
Hyperthermic treatment of Bowen's disease with disposable chemical pocket warmers: a report of 8 cases.
J Am Acad Dermatol. 2000 Dec;43(6):1070-5. doi: 10.1067/mjd.2000.111351.
Abstract/Text Bowen's disease is a form of squamous cell carcinoma in situ, in which local hyperthermia may be efficacious. We studied 8 patients with Bowen's disease to ascertain whether hyperthermia can be effective against it. As a heat source, disposable chemical pocket warmers were applied daily with pressure directly to the lesion site while the patient was awake, and the clinical course was observed for 4 to 5 months. The lesion was then excised and examined to determine the histopathologic effects. The results showed efficacy in 6 cases, in which the nodular and invasive lesions and the erythematous patches abated; then the lesions disappeared, leaving deposits of pigment (complete remission). In one case, the signs improved by at least 50% (partial remission); in the other case, there was only slight palliation (no response). As for the posttreatment histopathologic effects, tumor cells were eliminated in 3 cases, isolated tumor cells were seen in 3 cases, and there was no change in 2. Although the treatment did not yield perfect results, it represents a major improvement of hyperthermic therapy and is one effective method of treating Bowen's disease.

PMID 11100025
薬剤監修について:
オーダー内の薬剤用量は日本医科大学付属病院 薬剤部 部長 伊勢雄也 以下、渡邉裕次、井ノ口岳洋、梅田将光および日本医科大学多摩永山病院 副薬剤部長 林太祐による疑義照会のプロセスを実施、疑義照会の対象については著者の方による再確認を実施しております。
※薬剤中分類、用法、同効薬、診療報酬は、エルゼビアが独自に作成した薬剤情報であり、 著者により作成された情報ではありません。
尚、用法は添付文書より、同効薬は、薬剤師監修のもとで作成しております。
※同効薬・小児・妊娠および授乳中の注意事項等は、海外の情報も掲載しており、日本の医療事情に適応しない場合があります。
※薬剤情報の(適外/適内/⽤量内/⽤量外/㊜)等の表記は、エルゼビアジャパン編集部によって記載日時にレセプトチェックソフトなどで確認し作成しております。ただし、これらの記載は、実際の保険適応の査定において保険適応及び保険適応外と判断されることを保証するものではありません。また、検査薬、輸液、血液製剤、全身麻酔薬、抗癌剤等の薬剤は保険適応の記載の一部を割愛させていただいています。
(詳細はこちらを参照)
著者のCOI(Conflicts of Interest)開示:
清原隆宏 : 特に申告事項無し[2024年]
監修:戸倉新樹 : 講演料(サノフィ(株),日本イーライリリー(株),アッヴィ合同会社,協和キリン(株))[2024年]

ページ上部に戻る

ボーエン病

戻る