Abstract

Eosinophilic granuloma (EG) is the unifocal osseous form of Langerhans cell histiocytosis (LCH), which usually affects the skull and long bones. Although it most commonly affects the pediatric age group, it can rarely be seen in adults. Skeletal involvement is common in adult patients, but isolated rib involvement is extremely rare. Differential diagnosis includes other osteolytic lesions such as Ewing’s sarcoma, tuberculosis, multiple myeloma, lymphoma, and primary bone malignancy.The diagnosis must be confirmed histopathologically. In addition to pathological Langerhans cells, inflammatory cells such as lymphocytes, eosinophils, and macrophages are observed in microscopy. Immunohistochemically, CD1a, S-100, and Langerin positivity are observed in biopsy and/or surgical excision material.Treatment options may vary depending on the localization and extent of the disease. In unifocal EG, close observation of the patient may be preferred, as well as surgical excision, radiotherapy, and intra-lesional steroid administration. The prognosis in patients with a single bone lesion is quite good compared to other groups.In this case report, we present a metachronous EG of rib developed in two different ribs by an interval of seven years, which were both surgically treated. In this mild variant of LCH, surgical resection with clean margins has a favorable outcome without the need for additional adjuvant therapy. Metachronous tumors may develop in isolated unifocal bone EGs, and long-term follow-up is mandatory.

Highlights

  • We present a metachronous Eosinophilic granuloma (EG) of rib developed in two different ribs by an interval of seven years, which were both surgically treated

  • Metachronous tumors may develop in isolated unifocal bone EGs, and long-term follow-up is mandatory

  • Langerhans cell histiocytosis (LCH) is an idiopathic disease that occurs as a result of the localized or widespread accumulation of Langerhans cells originating in the bone marrow in various tissues for an unknown reason [1]

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Summary

Introduction

Langerhans cell histiocytosis (LCH) is an idiopathic disease that occurs as a result of the localized or widespread accumulation of Langerhans cells originating in the bone marrow in various tissues for an unknown reason [1] It most commonly affects the pediatric age group, it can rarely be seen in adults. A 39-year-old male patient, admitted with chest pain in 2014, was found to have an expansile lesion in the left fifth rib in his radiological examinations, and surgical resection was decided (Figure 1). F-18 fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) showed pathological uptake (SUVmax: 6,5) in the lytic lesion in the left fourth rib and changes secondary to the previous operation in the anterolateral arcs of the left fifth to sixth ribs (Figure 4). The patient was doing well in his second month of follow-up

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