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Erschienen in: European Journal of Nuclear Medicine and Molecular Imaging 11/2023

Open Access 26.05.2023 | Image of the Month

Granulomatous dermatitis: a rare pitfall in lymphoma staging with [18F]FDG-PET/CT

verfasst von: Johanna S. Enke, Alexander Gäble, Nic G. Reitsam, Tina Schaller, Martin Trepel, Klaus Hirschbühl, Julia Welzel, Alexander Dierks, Malte Kircher, Constantin Lapa

Erschienen in: European Journal of Nuclear Medicine and Molecular Imaging | Ausgabe 11/2023

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A 36-year-old male with anaplastic large T cell lymphoma (A; nodal manifestations in the left iliac and left inguinal region, arrow) who had received six cycles of chemotherapy (brentuximab vedotin, cyclophosphamide, doxorubicin, and prednisone) presented for restaging prior to autologous stem cell transplantation. A few days earlier, the patient had noticed multiple new tender subcutaneous nodules, and erythemato-squamous, polymorphous, partially atrophic plaques all over his body (B1). [18F]FDG-positron emission tomography/computed tomography (PET/CT) showed complete metabolic response of primary lymphoma manifestations but revealed intense tracer accumulation in the disseminated subcutaneous nodules (B, axial image B2). Besides cutaneous involvement by T cell lymphoma, differential diagnoses included cutaneous sarcoidosis and pityriasis rosea. Biopsy of a subcutaneous nodule revealed no evidence of malignancy but granulomatous inflammation (B3) most consistent with reactive granulomatous dermatitis. After initiation of prednisone therapy, all (sub-)cutaneous lesions quickly resolved, and the patient was eligible for stem cell transplantation. Follow-up [18F]FDG-PET/CT demonstrated only residual tracer uptake of some lesions and a sustained complete lymphoma response (C).
Reactive granulomatous dermatitis is a very rare skin disease with only several hundred cases reported worldwide so far [1], most commonly associated with autoimmune disorders such as rheumatoid arthritis. Furthermore, it has been associated with hematologic malignancies, including — in approximately 3% of cases — (B cell) lymphoma [13]. To our knowledge, this is one of the very first cases of granulomatous dermatitis in anaplastic large T cell lymphoma [4], and the first visualization of granulomatous dermatitis by [18F]FDG-PET/CT mimicking cutaneous lymphoma manifestations.

Declarations

Written informed consent for publication of this report and accompanying images was obtained from the patient.

Conflict of interest

The authors declare no competing interests.
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Literatur
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Zurück zum Zitat Bangalore Kumar A, Lehman JS, Johnson EF, et al. Reactive granulomatous dermatitis as a clinically relevant and unifying term: a retrospective review of clinical features, associated systemic diseases, histopathology and treatment for a series of 65 patients at Mayo Clinic. J Eur Acad Dermatol Venereol. 2022;36(12):2443–50. https://doi.org/10.1111/jdv.18203.CrossRefPubMed Bangalore Kumar A, Lehman JS, Johnson EF, et al. Reactive granulomatous dermatitis as a clinically relevant and unifying term: a retrospective review of clinical features, associated systemic diseases, histopathology and treatment for a series of 65 patients at Mayo Clinic. J Eur Acad Dermatol Venereol. 2022;36(12):2443–50. https://​doi.​org/​10.​1111/​jdv.​18203.CrossRefPubMed
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Zurück zum Zitat Calonje JE, Greaves MW. Cutaneous extravascular necrotizing granuloma (Churg-Strauss) as a paraneoplastic manifestation of non-Hodgkin’s B-cell lymphoma. J R Soc Med. 1993;86(9):549–50.PubMedPubMedCentral Calonje JE, Greaves MW. Cutaneous extravascular necrotizing granuloma (Churg-Strauss) as a paraneoplastic manifestation of non-Hodgkin’s B-cell lymphoma. J R Soc Med. 1993;86(9):549–50.PubMedPubMedCentral
Metadaten
Titel
Granulomatous dermatitis: a rare pitfall in lymphoma staging with [18F]FDG-PET/CT
verfasst von
Johanna S. Enke
Alexander Gäble
Nic G. Reitsam
Tina Schaller
Martin Trepel
Klaus Hirschbühl
Julia Welzel
Alexander Dierks
Malte Kircher
Constantin Lapa
Publikationsdatum
26.05.2023
Verlag
Springer Berlin Heidelberg
Erschienen in
European Journal of Nuclear Medicine and Molecular Imaging / Ausgabe 11/2023
Print ISSN: 1619-7070
Elektronische ISSN: 1619-7089
DOI
https://doi.org/10.1007/s00259-023-06284-3

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