Literature DB >> 26411178

Langerhans Cell Histiocytosis of the Bone Presenting as Back Pain: An Unusual Diagnosis for a Common Complaint.

Elena Gkrouzman, René H Cuadra, Jason Jacob.   

Abstract

Langerhans cell histiocytosis (LCH) is a rare disease entity characterized by histiocyte infiltration of various organ systems with abroad spectrum of clinical manifestations and prognosis, ranging from benign and self-limiting to lethal. We report a case of a healthy 29-year-old male who presented with upper back pain that was unresponsive to over-the-counter analgesics. The painwas eventually attributed to a single lytic lesion at the posterolateral aspect of his seventh rib, consistent with LCH of the bone. Our patient's symptoms subsided without any surgical intervention apart from a biopsy that was performed for diagnostic purposes. His lytic lesion eventually regressed, and he has remained asymptomatic at follow-up. We provide a brief review of literature on diagnostic approach, guidelines, and treatment modalities for adults diagnosed with LCH of the bone, a rare diagnosis most frequently presenting with a common complaint such as back pain.

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Year:  2015        PMID: 26411178

Source DB:  PubMed          Journal:  Conn Med        ISSN: 0010-6178


  2 in total

1.  Diagnosis and treatment of adult Langerhans cell histiocytosis in the rib: a case report and literature review.

Authors:  Xin Li; Xufeng Liu; Daqiang Sun
Journal:  Ann Transl Med       Date:  2022-09

2.  Multifocal Langerhans cell histiocytosis in a child.

Authors:  Juna Musa; Abu Bakar Siddik; Ilir Ahmetgjekaj; Masum Rahman; Ali Guy; Abdur Rahman; Samar Ikram; Erisa Kola; Valon Vokshi; Eram Ahsan; Kristi Saliaj; Fjolla Hyseni
Journal:  Radiol Case Rep       Date:  2021-07-17
  2 in total

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