Li David G, Krajewski Katherine M, Mostaghimi Arash
Department of Dermatology, Brigham & Women's Hospital, Harvard Medical School, Boston, USA.
Department of Imaging, Dana-Farber Cancer Institute; Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, USA.
Cureus. 2018 Apr 12;10(4):e2466. doi: 10.7759/cureus.2466.
Cellulitis is a common skin and soft tissue infection with substantial misdiagnosis rates due to its nonspecific clinical characteristics. In this report, we present a patient with recurrent metastatic diffuse large B-cell lymphoma (DLBCL) masquerading as a unilateral lower extremity cellulitis. A 62-year-old man with a history of DLBCL, in remission for two years, presented with a two-week history of swelling and erythema of the right thigh and leg. Despite treatment with clindamycin and cephalexin, the redness and swelling continued to progress. On presentation to the emergency department, vitals were within normal limits, laboratory workup was significant only for borderline anemia and thrombocytopenia, and bilateral lower extremity ultrasound was negative for a clot. The patient was evaluated by a dermatologist who recommended further imaging workup for proximal vascular compression given the uniformity of inflammation and edema in the absence of fever or systemic symptoms. Imaging revealed retroperitoneal lymphadenopathy, right pelvic side wall and right inguinal lymphadenopathy, an intramuscular lymphomatous involvement of the right iliopsoas muscle, and mass compression of the right external iliac vein. Bone marrow and soft-tissue biopsies confirmed recurrent and metastatic DLBCL. In this patient, the atypical cellulitis-like features are likely due to venous and lymphatic obstruction secondary to mass effect from metastasis. Going forward, clinicians should consider compression-induced edema as a sign of primary or recurrent malignancy in patients with refractory or atypical cellulitis.
蜂窝织炎是一种常见的皮肤和软组织感染,因其非特异性临床特征而误诊率较高。在本报告中,我们介绍了一名复发性转移性弥漫性大B细胞淋巴瘤(DLBCL)患者,其症状伪装为单侧下肢蜂窝织炎。一名62岁男性,有DLBCL病史,已缓解两年,出现右大腿和小腿肿胀及红斑两周。尽管使用了克林霉素和头孢氨苄治疗,但红肿仍持续进展。到急诊科就诊时,生命体征正常,实验室检查仅显示临界贫血和血小板减少,双侧下肢超声检查未发现血栓。皮肤科医生对患者进行了评估,鉴于炎症和水肿均匀但无发热或全身症状,建议对近端血管受压情况进行进一步影像学检查。影像学检查显示腹膜后淋巴结肿大、右盆腔侧壁和右腹股沟淋巴结肿大、右髂腰肌肌肉内淋巴瘤累及以及右髂外静脉受压。骨髓和软组织活检证实为复发性转移性DLBCL。在该患者中,非典型蜂窝织炎样特征可能是由于转移瘤的占位效应导致静脉和淋巴阻塞。未来,临床医生应将压迫性水肿视为难治性或非典型蜂窝织炎患者原发性或复发性恶性肿瘤的迹象。