Get Permission Mall, Sharma, Marcus, and Yadav: Autoeczematization during radiation therapy – An unforeseen crumble


Case Report

A 73 year male who is a diagnosed case of non small cell carcinoma left lung with no known co-morbidity received 3 cycles of chemotherapy with Inj. Pemetrexed and Inj. Carboplatin had been referred to the OPD for radiation therapy. PET CT showed metabolically active pleural based soft tissue mass lesion in left lobe of lung (~ 2.8 x 4.1 x 4.6 cm with SUV max= 5.9). Patient was taken up for external beam radiation therapy to a dose of 60Gy/30 fractions at 2Gy per fraction by volumetric modulated arc therapy technique with 6MV X-rays. Patient developed eczematous skin lesion over bilateral hands after receiving 13 Fractions. The lesion appeared as scattered patchy macules and papules with thin raised plaques and peeling of skin that were non pruritic over his hands bilaterally (Figure 1). Radiation therapy was halted with immediate effect and a dermatological opinion was taken. Patient was adviced topical steroids and the ezema subsided in a week (Figure 2).

Figure 1

Autoeczematization or ID reaction developed over bilateral hands after 13 fractions of EBRT to the primary lung lesion.

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Figure 2

Reactions subsided after one week of topical treatment.

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Discussion

Autoeczematization or id reaction, is a disseminated eczematous reaction that occurs due to a release of antigen(s) after exposure to a primary stimulus, with the eczema spreading to a site distant from the original one. Whitfield1 first described the phenomenon in 1921, when he postulated that it was due to sensitization of the skin after a primary stimulus. He called it “a form of auto-intoxication derived from changes in the patient’s own tissues.”1 It develops at the cutaneous sites away from a primary inflammation focus and where the secondary acute dermatitis is not explained by the cause of the initial inflammation. Factors such as infection, trauma, irritant chemicals, and ionizing radiation are known to precipitate autosensitization. 2

The pathogenesis of autosensitization dermatitis is thought to be related with increased HLA-DR- and IL-2R-positive T lymphocytes 3 with the elevated ratio of helper to suppressor T lymphocytes 4 and with hematogenous dissemination of epidermal cytokines from a primary focus. 5 In our case of primary lesion of lung being treated with radiation therapy developed autoeczematization in bilateral hands i.e area distant from the radiation field.

Conclusion

We postulate that T cells are reactive to keratinocyte antigens that are produced during keratinocyte damage, which induce this autoeczematization. Recognition is important to prevent excessive and inappropriate investigation and treatment. Studies with current technology are needed to facilitate further understanding of this phenomenon. Given the rarity of such reactions during radiation therapy, this case report will definitely add a much-needed view point to treating oncologists towards investigating and managing similar cases. Furthermore, prospective case reports are warranted to confirm the diagnosis, mechanism and prevention.

Conflict of Interest

None.

Source of Funding

None.

References

1 

A Whitfield Lumleian Lectures on Some Points in the Aetiology of Skin Diseases. Delivered before the Royal College of Physicians of London on March 10th, 15th, and 17th, 1921Lancet192121227

2 

K Wolff LA Goldsmith SI Katz BA Gilchrest AS Palle DJ Leffell Fitzpatrick’s Dermatology in General Medicine7th Edn.McGraw-HillNew York20081678

3 

JS Kasteler MJ Petersen JE Vance JJ Zone Circulating activated T lymphocytes in autoeczematizationArch Dermatol199212867958

4 

MJ Cunningham JJ Zone MJ Petersen JA Green Circulating activated (DR-positive) T lymphocytes in a patient with autoeczematizationJ Am Acad Dermatol1986146103941

5 

IR Williams TS Kupper Immunity at the surface: Homeostatic mechanisms of the skin immune systemLife Sci199658181485507



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Article History

Received : 18-11-2022

Accepted : 19-12-2022


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https://doi.org/ 10.18231/j.ijmpo.2022.038


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