Hypertrophic lichenoid dermatitis immune‐related adverse event during combined immune checkpoint and exportin inhibitor therapy: A diagnostic pitfall for superficially invasive squamous cell carcinoma

Immune checkpoint inhibitors (ICIs) for cancer treatment have revolutionized the field of medicine. However, an unintended but frequent consequence of ICI therapy is the development of cutaneous immune‐related adverse events (irAEs), such as lichenoid dermatitis irAEs (LD‐irAEs). The hypertrophic va...

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Veröffentlicht in:Journal of cutaneous pathology 2020-10, Vol.47 (10), p.954-959
Hauptverfasser: Marques‐Piubelli, Mario L., Tetzlaff, Michael T., Nagarajan, Priyadharsini, Duke, Taylor C., Glitza Oliva, Isabella C., Ledesma, Debora A., Aung, Phyu P., Torres‐Cabala, Carlos A., Wistuba, Ignacio I., Prieto, Victor G., Nelson, Kelly C., Curry, Jonathan L.
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container_issue 10
container_start_page 954
container_title Journal of cutaneous pathology
container_volume 47
creator Marques‐Piubelli, Mario L.
Tetzlaff, Michael T.
Nagarajan, Priyadharsini
Duke, Taylor C.
Glitza Oliva, Isabella C.
Ledesma, Debora A.
Aung, Phyu P.
Torres‐Cabala, Carlos A.
Wistuba, Ignacio I.
Prieto, Victor G.
Nelson, Kelly C.
Curry, Jonathan L.
description Immune checkpoint inhibitors (ICIs) for cancer treatment have revolutionized the field of medicine. However, an unintended but frequent consequence of ICI therapy is the development of cutaneous immune‐related adverse events (irAEs), such as lichenoid dermatitis irAEs (LD‐irAEs). The hypertrophic variant of LD‐irAE may be a diagnostic challenge since it can mimic superficially invasive squamous cell carcinoma (SCC). A 79‐year‐old woman with metastatic melanoma who began treatment with an ICI—pembrolizumab—plus exportin‐1 (XPO1) inhibitor presented after 1 month of therapy with symmetrical violaceous papules coalescing into plaques and with two nodules of the bilateral dorsal hands. Biopsy of the nodules revealed an actinic keratosis and atypical epidermal proliferation concerning for SCC. However, in the ensuing 3 weeks, the patient developed multiple new erythematous, violaceous, and scaly macules and papules, some coalescing into plaques on the extremities. Biopsies of these lesions revealed exuberant irregular epidermal hyperplasia with hypermaturation and lichenoid infiltrate concentrated at the base of the elongated, broadened rete ridges, consistent with hypertrophic LD‐irAE. Treatment included topical fluocinonide ointment, intralesional triamcinolone injections and oral acitretin. Distinguishing hypertrophic LD‐irAE and SCC can be challenging since both entities share histopathologic features; thus, correlation with clinical presentation is essential for diagnosis and optimal patient management.
doi_str_mv 10.1111/cup.13739
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However, an unintended but frequent consequence of ICI therapy is the development of cutaneous immune‐related adverse events (irAEs), such as lichenoid dermatitis irAEs (LD‐irAEs). The hypertrophic variant of LD‐irAE may be a diagnostic challenge since it can mimic superficially invasive squamous cell carcinoma (SCC). A 79‐year‐old woman with metastatic melanoma who began treatment with an ICI—pembrolizumab—plus exportin‐1 (XPO1) inhibitor presented after 1 month of therapy with symmetrical violaceous papules coalescing into plaques and with two nodules of the bilateral dorsal hands. Biopsy of the nodules revealed an actinic keratosis and atypical epidermal proliferation concerning for SCC. However, in the ensuing 3 weeks, the patient developed multiple new erythematous, violaceous, and scaly macules and papules, some coalescing into plaques on the extremities. Biopsies of these lesions revealed exuberant irregular epidermal hyperplasia with hypermaturation and lichenoid infiltrate concentrated at the base of the elongated, broadened rete ridges, consistent with hypertrophic LD‐irAE. Treatment included topical fluocinonide ointment, intralesional triamcinolone injections and oral acitretin. Distinguishing hypertrophic LD‐irAE and SCC can be challenging since both entities share histopathologic features; thus, correlation with clinical presentation is essential for diagnosis and optimal patient management.</description><identifier>ISSN: 0303-6987</identifier><identifier>EISSN: 1600-0560</identifier><identifier>DOI: 10.1111/cup.13739</identifier><identifier>PMID: 32394425</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject><![CDATA[Acitretin - administration & dosage ; Acitretin - therapeutic use ; Aged ; Antibodies, Monoclonal, Humanized - adverse effects ; Antibodies, Monoclonal, Humanized - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; anti‐PD‐1/PD‐L1 therapy ; Biopsy ; Carcinoma, Squamous Cell ; Dermatitis ; Dermatitis - immunology ; Dermatitis - pathology ; Drug Eruptions - pathology ; Drug Therapy, Combination ; Exportin 1 Protein ; Female ; Fluocinonide - administration & dosage ; Fluocinonide - therapeutic use ; Glucocorticoids - administration & dosage ; Glucocorticoids - therapeutic use ; Humans ; Hyperplasia ; hypertrophic lichenoid dermatitis ; Hypertrophy - pathology ; Immune checkpoint inhibitors ; Immune Checkpoint Inhibitors - adverse effects ; immune‐related adverse event ; Invasiveness ; Karyopherins - adverse effects ; Karyopherins - antagonists & inhibitors ; Karyopherins - therapeutic use ; Keratolytic Agents - administration & dosage ; Keratolytic Agents - therapeutic use ; Keratosis ; Lichenoid Eruptions - chemically induced ; Lichenoid Eruptions - immunology ; Lichenoid Eruptions - pathology ; Melanoma ; Melanoma - drug therapy ; Melanoma - secondary ; Metastases ; Monoclonal antibodies ; Patients ; Pembrolizumab ; Plaques ; Programmed Cell Death 1 Receptor - antagonists & inhibitors ; Receptors, Cytoplasmic and Nuclear - antagonists & inhibitors ; Squamous cell carcinoma ; Targeted cancer therapy ; Treatment Outcome ; Triamcinolone - administration & dosage ; Triamcinolone - therapeutic use ; XPO1 inhibitor]]></subject><ispartof>Journal of cutaneous pathology, 2020-10, Vol.47 (10), p.954-959</ispartof><rights>2020 John Wiley &amp; Sons A/S. 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However, an unintended but frequent consequence of ICI therapy is the development of cutaneous immune‐related adverse events (irAEs), such as lichenoid dermatitis irAEs (LD‐irAEs). The hypertrophic variant of LD‐irAE may be a diagnostic challenge since it can mimic superficially invasive squamous cell carcinoma (SCC). A 79‐year‐old woman with metastatic melanoma who began treatment with an ICI—pembrolizumab—plus exportin‐1 (XPO1) inhibitor presented after 1 month of therapy with symmetrical violaceous papules coalescing into plaques and with two nodules of the bilateral dorsal hands. Biopsy of the nodules revealed an actinic keratosis and atypical epidermal proliferation concerning for SCC. However, in the ensuing 3 weeks, the patient developed multiple new erythematous, violaceous, and scaly macules and papules, some coalescing into plaques on the extremities. Biopsies of these lesions revealed exuberant irregular epidermal hyperplasia with hypermaturation and lichenoid infiltrate concentrated at the base of the elongated, broadened rete ridges, consistent with hypertrophic LD‐irAE. Treatment included topical fluocinonide ointment, intralesional triamcinolone injections and oral acitretin. Distinguishing hypertrophic LD‐irAE and SCC can be challenging since both entities share histopathologic features; thus, correlation with clinical presentation is essential for diagnosis and optimal patient management.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>32394425</pmid><doi>10.1111/cup.13739</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-0630-6222</orcidid><orcidid>https://orcid.org/0000-0002-3398-0573</orcidid><orcidid>https://orcid.org/0000-0002-6324-2096</orcidid><orcidid>https://orcid.org/0000-0001-7422-0661</orcidid><orcidid>https://orcid.org/0000-0002-5346-2669</orcidid></addata></record>
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subjects Acitretin - administration & dosage
Acitretin - therapeutic use
Aged
Antibodies, Monoclonal, Humanized - adverse effects
Antibodies, Monoclonal, Humanized - therapeutic use
Antineoplastic Combined Chemotherapy Protocols - adverse effects
anti‐PD‐1/PD‐L1 therapy
Biopsy
Carcinoma, Squamous Cell
Dermatitis
Dermatitis - immunology
Dermatitis - pathology
Drug Eruptions - pathology
Drug Therapy, Combination
Exportin 1 Protein
Female
Fluocinonide - administration & dosage
Fluocinonide - therapeutic use
Glucocorticoids - administration & dosage
Glucocorticoids - therapeutic use
Humans
Hyperplasia
hypertrophic lichenoid dermatitis
Hypertrophy - pathology
Immune checkpoint inhibitors
Immune Checkpoint Inhibitors - adverse effects
immune‐related adverse event
Invasiveness
Karyopherins - adverse effects
Karyopherins - antagonists & inhibitors
Karyopherins - therapeutic use
Keratolytic Agents - administration & dosage
Keratolytic Agents - therapeutic use
Keratosis
Lichenoid Eruptions - chemically induced
Lichenoid Eruptions - immunology
Lichenoid Eruptions - pathology
Melanoma
Melanoma - drug therapy
Melanoma - secondary
Metastases
Monoclonal antibodies
Patients
Pembrolizumab
Plaques
Programmed Cell Death 1 Receptor - antagonists & inhibitors
Receptors, Cytoplasmic and Nuclear - antagonists & inhibitors
Squamous cell carcinoma
Targeted cancer therapy
Treatment Outcome
Triamcinolone - administration & dosage
Triamcinolone - therapeutic use
XPO1 inhibitor
title Hypertrophic lichenoid dermatitis immune‐related adverse event during combined immune checkpoint and exportin inhibitor therapy: A diagnostic pitfall for superficially invasive squamous cell carcinoma
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