Bullous mycosis fungoides: Report of a case complicated by Kaposi's varicelliform eruption

Vesiculobullous eruptions in mycosis fungoides (MF) are extremely rare. Here, we report a case of a 62‐year‐old woman presenting with erythematous patches and plaques of 2 years in duration, who had recently developed vesicles on erythematous MF plaques. Histopathological examination showed intra‐su...

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Vydané v:Journal of dermatology Ročník 40; číslo 10; s. 844 - 847
Hlavní autori: Xu, Xiu-Lian, Huang, Ying-Xue, Lin, Lin, Zhang, Meng-Li, Jiang, Yi-Qun, Sun, Jian-Fang
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: England Blackwell Publishing Ltd 01.10.2013
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ISSN:0385-2407, 1346-8138, 1346-8138
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Abstract Vesiculobullous eruptions in mycosis fungoides (MF) are extremely rare. Here, we report a case of a 62‐year‐old woman presenting with erythematous patches and plaques of 2 years in duration, who had recently developed vesicles on erythematous MF plaques. Histopathological examination showed intra‐subepidermal blisters, and infiltration of the epidermis by atypical lymphoid cells, forming Pautrier's microabscesses. Negative immunofluorescence excluded autoimmune blistering diseases. Immunohistochemistry revealed a CD4+ T‐cell phenotype and gene rearrangement study confirmed a clonal T‐cell proliferation. Kaposi's varicelliform eruption (KVE) developed in the patient 1 week after initiation of systemic corticosteroids and immunotherapy. Cluster of vesicles and erosions arising on the pre‐existing plaque and a positive immunofluorescence test for Herpes simplex virus and histopathological examination confirmed the diagnosis of cutaneous herpes infection. This is the first case report on bullous MF complicated by KVE in the published work.
AbstractList Vesiculobullous eruptions in mycosis fungoides (MF) are extremely rare. Here, we report a case of a 62-year-old woman presenting with erythematous patches and plaques of 2 years in duration, who had recently developed vesicles on erythematous MF plaques. Histopathological examination showed intra-subepidermal blisters, and infiltration of the epidermis by atypical lymphoid cells, forming Pautrier's microabscesses. Negative immunofluorescence excluded autoimmune blistering diseases. Immunohistochemistry revealed a CD4+ T-cell phenotype and gene rearrangement study confirmed a clonal T-cell proliferation. Kaposi's varicelliform eruption (KVE) developed in the patient 1 week after initiation of systemic corticosteroids and immunotherapy. Cluster of vesicles and erosions arising on the pre-existing plaque and a positive immunofluorescence test for Herpes simplex virus and histopathological examination confirmed the diagnosis of cutaneous herpes infection. This is the first case report on bullous MF complicated by KVE in the published work.
Vesiculobullous eruptions in mycosis fungoides (MF) are extremely rare. Here, we report a case of a 62-year-old woman presenting with erythematous patches and plaques of 2 years in duration, who had recently developed vesicles on erythematous MF plaques. Histopathological examination showed intra-subepidermal blisters, and infiltration of the epidermis by atypical lymphoid cells, forming Pautrier's microabscesses. Negative immunofluorescence excluded autoimmune blistering diseases. Immunohistochemistry revealed a CD4⁺ T-cell phenotype and gene rearrangement study confirmed a clonal T-cell proliferation. Kaposi's varicelliform eruption (KVE) developed in the patient 1 week after initiation of systemic corticosteroids and immunotherapy. Cluster of vesicles and erosions arising on the pre-existing plaque and a positive immunofluorescence test for Herpes simplex virus and histopathological examination confirmed the diagnosis of cutaneous herpes infection. This is the first case report on bullous MF complicated by KVE in the published work.
Vesiculobullous eruptions in mycosis fungoides (MF) are extremely rare. Here, we report a case of a 62-year-old woman presenting with erythematous patches and plaques of 2 years in duration, who had recently developed vesicles on erythematous MF plaques. Histopathological examination showed intra-subepidermal blisters, and infiltration of the epidermis by atypical lymphoid cells, forming Pautrier's microabscesses. Negative immunofluorescence excluded autoimmune blistering diseases. Immunohistochemistry revealed a CD4⁺ T-cell phenotype and gene rearrangement study confirmed a clonal T-cell proliferation. Kaposi's varicelliform eruption (KVE) developed in the patient 1 week after initiation of systemic corticosteroids and immunotherapy. Cluster of vesicles and erosions arising on the pre-existing plaque and a positive immunofluorescence test for Herpes simplex virus and histopathological examination confirmed the diagnosis of cutaneous herpes infection. This is the first case report on bullous MF complicated by KVE in the published work.Vesiculobullous eruptions in mycosis fungoides (MF) are extremely rare. Here, we report a case of a 62-year-old woman presenting with erythematous patches and plaques of 2 years in duration, who had recently developed vesicles on erythematous MF plaques. Histopathological examination showed intra-subepidermal blisters, and infiltration of the epidermis by atypical lymphoid cells, forming Pautrier's microabscesses. Negative immunofluorescence excluded autoimmune blistering diseases. Immunohistochemistry revealed a CD4⁺ T-cell phenotype and gene rearrangement study confirmed a clonal T-cell proliferation. Kaposi's varicelliform eruption (KVE) developed in the patient 1 week after initiation of systemic corticosteroids and immunotherapy. Cluster of vesicles and erosions arising on the pre-existing plaque and a positive immunofluorescence test for Herpes simplex virus and histopathological examination confirmed the diagnosis of cutaneous herpes infection. This is the first case report on bullous MF complicated by KVE in the published work.
Vesiculobullous eruptions in mycosis fungoides (MF) are extremely rare. Here, we report a case of a 62‐year‐old woman presenting with erythematous patches and plaques of 2 years in duration, who had recently developed vesicles on erythematous MF plaques. Histopathological examination showed intra‐subepidermal blisters, and infiltration of the epidermis by atypical lymphoid cells, forming Pautrier's microabscesses. Negative immunofluorescence excluded autoimmune blistering diseases. Immunohistochemistry revealed a CD4+ T‐cell phenotype and gene rearrangement study confirmed a clonal T‐cell proliferation. Kaposi's varicelliform eruption (KVE) developed in the patient 1 week after initiation of systemic corticosteroids and immunotherapy. Cluster of vesicles and erosions arising on the pre‐existing plaque and a positive immunofluorescence test for Herpes simplex virus and histopathological examination confirmed the diagnosis of cutaneous herpes infection. This is the first case report on bullous MF complicated by KVE in the published work.
Vesiculobullous eruptions in mycosis fungoides (MF) are extremely rare. Here, we report a case of a 62-year-old woman presenting with erythematous patches and plaques of 2 years in duration, who had recently developed vesicles on erythematous MF plaques. Histopathological examination showed intra-subepidermal blisters, and infiltration of the epidermis by atypical lymphoid cells, forming Pautrier's microabscesses. Negative immunofluorescence excluded autoimmune blistering diseases. Immunohistochemistry revealed a CD4+ T-cell phenotype and gene rearrangement study confirmed a clonal T-cell proliferation. Kaposi's varicelliform eruption (KVE) developed in the patient 1 week after initiation of systemic corticosteroids and immunotherapy. Cluster of vesicles and erosions arising on the pre-existing plaque and a positive immunofluorescence test for Herpes simplex virus and histopathological examination confirmed the diagnosis of cutaneous herpes infection. This is the first case report on bullous MF complicated by KVE in the published work. [PUBLICATION ABSTRACT]
Author Huang, Ying-Xue
Sun, Jian-Fang
Xu, Xiu-Lian
Lin, Lin
Zhang, Meng-Li
Jiang, Yi-Qun
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  email: jfsun_pumcderm@yahoo.com.cn
  organization: Institute of Dermatology, Chinese Academy of Medical Sciences, Nanjing, China
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mycosis fungoides
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References_xml – reference: Segal RJ, Watson W. Kaposi's varicelliform eruption in mycosis fungoides. Arch Dermatol 1978; 114: 1067-1069.
– reference: Pullmann H, Trost T, Witte U. Acral bullae following puva-therapy (author's transl). Z Hautkr 1982; 57: 288-293.
– reference: Ueda C, Makino T, Asano Y, Watanabe H, Hanakawa H, Shimizu T. An ultrastructural examination of a blistering lesion of mycosis fungoides bullosa. Br J Dermatol 2011; 165: 213-214.
– reference: Sarnoff DS, DeFeo CP. Coexistence of pemphigus foliaceus and mycosis fungoides. Arch Dermatol 1985; 121: 669-672.
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– reference: Kaposi M. "Mycosis fungoides" und ihre beziehungen zu anderen ahnlichen erkrankungsformen. Wien Med Wochenschr 1887; 19: 22-37.
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– reference: Turner CC, Assaad D, Shear NH. Bullae on the legs of an elderly man. Mycosis fungoides bullosa. Arch Dermatol 1994; 130: 1551-1552, 1554-1555.
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– volume: 192
  start-page: 50
  year: 1996
  end-page: 55
  article-title: Long‐term interferon‐alpha therapy induces autoantibodies against epidermis
  publication-title: Dermatology
– volume: 138
  start-page: 141
  year: 1998
  end-page: 144
  article-title: Vesicular mycosis fungoides
  publication-title: Br J Dermatol
– volume: 57
  start-page: 1757
  year: 1982
  end-page: 1765
  article-title: Generalized cutaneous herpes infection in mycosis fungoides (Kaposi's varicelliform eruption)
  publication-title: Z Hautkr
– volume: 121
  start-page: 669
  year: 1985
  end-page: 672
  article-title: Coexistence of pemphigus foliaceus and mycosis fungoides
  publication-title: Arch Dermatol
– volume: 114
  start-page: 1067
  year: 1978
  end-page: 1069
  article-title: Kaposi's varicelliform eruption in mycosis fungoides
  publication-title: Arch Dermatol
– volume: 165
  start-page: 213
  year: 2011
  end-page: 214
  article-title: An ultrastructural examination of a blistering lesion of mycosis fungoides bullosa
  publication-title: Br J Dermatol
– volume: 48
  start-page: 359
  year: 1943
  end-page: 368
  article-title: Mycosis fungoides with bullous lesions: report of a case resistant to roentgen and arsenical therapy; effects of empiric therapy, partly based on laboratory investigations
  publication-title: Arch Derm Syphilol
– volume: 24
  start-page: 173
  year: 1985
  end-page: 176
  article-title: Bullous pemphigoid. Occurrence in a patient with mycosis fungoides receiving puva and topical nitrogen mustard therapy
  publication-title: Int J Dermatol
– volume: 22
  start-page: 306
  year: 1990
  end-page: 307
  article-title: Local bullous reaction to topical mechlorethamine (mustine)
  publication-title: Contact Dermatitis
– volume: 57
  start-page: 288
  year: 1982
  end-page: 293
  article-title: Acral bullae following puva‐therapy (author's transl)
  publication-title: Z Hautkr
– volume: 15
  start-page: 641
  year: 1988
  end-page: 645
  article-title: Total skin electron irradiation for mycosis fungoides: relationship between acute toxicities and measured dose at different anatomic sites
  publication-title: Int J Radiat Oncol Biol Phys
– volume: 45
  start-page: 934
  year: 2001
  end-page: 839
  article-title: Mycosis fungoides bullosa: report of a case and review of the literature
  publication-title: J Am Acad Dermatol
– volume: 22
  start-page: 41
  year: 1997
  end-page: 43
  article-title: Kaposi's varicelliform eruption in a patient with mycosis fungoides
  publication-title: Clin Exp Dermatol
– volume: 19
  start-page: 22
  year: 1887
  end-page: 37
  article-title: “Mycosis fungoides” und ihre beziehungen zu anderen ahnlichen erkrankungsformen
  publication-title: Wien Med Wochenschr
– volume: 130
  start-page: 1551
  year: 1994
  end-page: 1552
  article-title: Bullae on the legs of an elderly man. Mycosis fungoides bullosa
  publication-title: Arch Dermatol
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Snippet Vesiculobullous eruptions in mycosis fungoides (MF) are extremely rare. Here, we report a case of a 62‐year‐old woman presenting with erythematous patches and...
Vesiculobullous eruptions in mycosis fungoides (MF) are extremely rare. Here, we report a case of a 62-year-old woman presenting with erythematous patches and...
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StartPage 844
SubjectTerms bullous
CD4 antigen
Female
Herpes simplex virus
Humans
immunohistochemistry
Kaposi Varicelliform Eruption - complications
Kaposi Varicelliform Eruption - pathology
Kaposi's varicelliform
Middle Aged
mycosis fungoides
Mycosis Fungoides - complications
Mycosis Fungoides - pathology
Skin - pathology
Title Bullous mycosis fungoides: Report of a case complicated by Kaposi's varicelliform eruption
URI https://api.istex.fr/ark:/67375/WNG-H3FNK1QT-Z/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2F1346-8138.12253
https://www.ncbi.nlm.nih.gov/pubmed/23961851
https://www.proquest.com/docview/1439165807
https://www.proquest.com/docview/1443397973
https://www.proquest.com/docview/1464497553
Volume 40
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