Cutaneous sarcoidosis following complete remission of diffuse large B-cell lymphoma: a case report and literature review

Sarcoidosis is a multi-systemic granulomatous disease of unknown etiology. Its association with lymphoproliferative disorders is termed sarcoidosis-lymphoma syndrome, which is typically characterized by sarcoidosis preceding lymphoma. However, the development of sarcoidosis after lymphoma remission is rare. A 72-year-old woman with a history of diffuse large B-cell lymphoma, treated 11 years earlier, was admitted with a rash and weakness in the lower limbs. Multiple inflammatory lesions, predominantly in the lower limbs, were detected using computed tomography and fluorodeoxyglucose positron emission tomography, and a diagnosis of systemic sarcoidosis was established <i>via</i> biopsies of the skin lesion. We reviewed 11 cases of sarcoidosis with cutaneous manifestations after lymphoma treatment, including the present case. In addition, we emphasized the importance of considering cutaneous sarcoidosis in the differential diagnosis of post-treatment skin lesions alongside lymphoma recurrence, as well as the need for histopathological confirmation.

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Journal
Immunological Medicine
Published
2025-10-29
DOI
https://doi.org/10.1080/25785826.2025.2576289
Primary Topic
Sarcoidosis and Beryllium Toxicity Research
Type
article
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Cutaneous sarcoidosis following complete remission of diffuse large B-cell lymphoma: a case report and literature review

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Sarcoidosis and Beryllium Toxicity Research
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Cutaneous sarcoidosis following complete remission of diffuse large B-cell lymphoma: a case report and literature review

Shuzo Sato, Yasuhiro Shimojima, Michiyuki Hakozaki, Kenji Saito, Yuya Sumichika, Shotaro Ogawa, Jumpei Temmoku, Kiyoshi Migita, Shuhei Yoshida, Erina Suzuki, Toshiyuki Yamamoto, Haruki Matsumoto, Ryuto Mukaiyama, Tomoyuki Asano, Yuko Hashimoto
article en

Abstract

Sarcoidosis is a multi-systemic granulomatous disease of unknown etiology. Its association with lymphoproliferative disorders is termed sarcoidosis-lymphoma syndrome, which is typically characterized by sarcoidosis preceding lymphoma. However, the development of sarcoidosis after lymphoma remission is rare. A 72-year-old woman with a history of diffuse large B-cell lymphoma, treated 11 years earlier, was admitted with a rash and weakness in the lower limbs. Multiple inflammatory lesions, predominantly in the lower limbs, were detected using computed tomography and fluorodeoxyglucose positron emission tomography, and a diagnosis of systemic sarcoidosis was established <i>via</i> biopsies of the skin lesion. We reviewed 11 cases of sarcoidosis with cutaneous manifestations after lymphoma treatment, including the present case. In addition, we emphasized the importance of considering cutaneous sarcoidosis in the differential diagnosis of post-treatment skin lesions alongside lymphoma recurrence, as well as the need for histopathological confirmation.

Immunological Medicine
Fukushima Medical University (JP), St Francis’ Hospital (ZM), St Francis Chronic Hospital (ZA), St. Francis Referral Hospital (TZ), Naggalama Hospital (UG)
Openalex Percentile: Top 61%
Sarcoidosis and Beryllium Toxicity Research
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