Scholarlink

Background <p>Erythema multiforme is a rare immune-mediated cutaneous disorder. Canine erythema multiforme (EM) can occur secondarily to triggers such as drugs, food and infections but is more commonly considered idiopathic. In humans, a paraneoplastic origin is also described whereas paraneoplastic EM has only been reported in one dog with thymoma. This case report is the first description of a dog with EM concurrently diagnosed with low-grade small-cell T-cell intestinal lymphoma, raising the suspicion of a paraneoplastic syndrome.</p> Case presentation <p>A 9-year-old, neutered male, crossbred dog, with no history of travel outside the United Kingdom or recent drug administration presented with progressive cutaneous lesions, pyrexia, lethargy, vomiting, and weight loss. Cutaneous lesions were generalised and consisted of multifocal to confluent erythematous macules and focally extensive variably sized patches of moderate to severe erythema and crusting, with ulceration. Histopathology was consistent with EM. Computed tomography identified a jejunal mass associated with jejunal lymphadenomegaly. The intestinal mass was excised and the enlarged non-resectable lymph node was biopsied. Histopathology, immunohistochemistry and PCR for antigen receptor rearrangement were consistent with transmural small-cell low-grade T-cell intestinal lymphoma with nodal involvement.</p> <p>Methylprednisolone and chlorambucil were initiated leading to complete resolution of the dermatological and gastrointestinal signs. Both drugs were progressively tapered and discontinued. During and post-treatment, repeat abdominal imaging with cytology and flow cytometry of the persistently mildly enlarged jejunal lymph node showed no evidence of lymphoma. Six months following chlorambucil discontinuation there was a recurrence of the cutaneous lesions with severe systemic deterioration, suggesting EM relapse. No triggers were identified. Repeat staging was declined and euthanasia was performed, 26&#xa0;months following initial diagnosis.</p> Conclusions <p>This is the first case reporting the concomitant occurrence of EM and small-cell lymphoma in a dog. While the relationship between these two diseases remains uncertain, a paraneoplastic disease was possible. This case highlights the importance of thorough investigations when canine EM is diagnosed, and an idiopathic origin is suspected.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Concomitant erythema multiforme in a dog with small-cell T-cell intestinal lymphoma: coincidence or paraneoplastic syndrome?

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年1月9日

查看全文
  • Eleanor K. Wyatt,
  • Malgorzata Ossowska,
  • Richard Blundell,
  • Petra Bizikova,
  • Vanessa Schmidt,
  • Jean-Benoit Tanis

摘要

Background

Erythema multiforme is a rare immune-mediated cutaneous disorder. Canine erythema multiforme (EM) can occur secondarily to triggers such as drugs, food and infections but is more commonly considered idiopathic. In humans, a paraneoplastic origin is also described whereas paraneoplastic EM has only been reported in one dog with thymoma. This case report is the first description of a dog with EM concurrently diagnosed with low-grade small-cell T-cell intestinal lymphoma, raising the suspicion of a paraneoplastic syndrome.

Case presentation

A 9-year-old, neutered male, crossbred dog, with no history of travel outside the United Kingdom or recent drug administration presented with progressive cutaneous lesions, pyrexia, lethargy, vomiting, and weight loss. Cutaneous lesions were generalised and consisted of multifocal to confluent erythematous macules and focally extensive variably sized patches of moderate to severe erythema and crusting, with ulceration. Histopathology was consistent with EM. Computed tomography identified a jejunal mass associated with jejunal lymphadenomegaly. The intestinal mass was excised and the enlarged non-resectable lymph node was biopsied. Histopathology, immunohistochemistry and PCR for antigen receptor rearrangement were consistent with transmural small-cell low-grade T-cell intestinal lymphoma with nodal involvement.

Methylprednisolone and chlorambucil were initiated leading to complete resolution of the dermatological and gastrointestinal signs. Both drugs were progressively tapered and discontinued. During and post-treatment, repeat abdominal imaging with cytology and flow cytometry of the persistently mildly enlarged jejunal lymph node showed no evidence of lymphoma. Six months following chlorambucil discontinuation there was a recurrence of the cutaneous lesions with severe systemic deterioration, suggesting EM relapse. No triggers were identified. Repeat staging was declined and euthanasia was performed, 26 months following initial diagnosis.

Conclusions

This is the first case reporting the concomitant occurrence of EM and small-cell lymphoma in a dog. While the relationship between these two diseases remains uncertain, a paraneoplastic disease was possible. This case highlights the importance of thorough investigations when canine EM is diagnosed, and an idiopathic origin is suspected.