Annals of Thoracic Medicine
LETTER TO THE EDITOR
Year
: 2010  |  Volume : 5  |  Issue : 3  |  Page : 178--179

Concurrent sternal and pulmonary foci of Langerhans cell histiocytosis


Young Hwan Koh, Hyeon Jong Moon, Byung-Su Kim, Dae Hee Han 
 Department of Radiology, Seoul St. Mary's Hospital, The Catholic University of Korea, 505, Banpo-dong, Seocho-gu, Seoul - 137 701, Korea

Correspondence Address:
Young Hwan Koh
Department of Radiology, Seoul St. Mary«SQ»s Hospital, The Catholic University of Korea, 505, Banpo-dong, Seocho-gu, Seoul - 137 701
Korea




How to cite this article:
Koh YH, Moon HJ, Kim BS, Han DH. Concurrent sternal and pulmonary foci of Langerhans cell histiocytosis.Ann Thorac Med 2010;5:178-179


How to cite this URL:
Koh YH, Moon HJ, Kim BS, Han DH. Concurrent sternal and pulmonary foci of Langerhans cell histiocytosis. Ann Thorac Med [serial online] 2010 [cited 2023 Mar 23 ];5:178-179
Available from: https://www.thoracicmedicine.org/text.asp?2010/5/3/178/65037


Full Text

Sir,

We recently came across a case of concurrent sternal and pulmonary langerhans cell histiocytosis (PLCH), who was successfully diagnosed by a careful review of high-resolution computed tomography (HRCT) and using ultrasound (US) guidance for tissue diagnosis. PLCH is part of the spectrum of the disorder manifesting as an interstitial lung disease [1] with an uncommon (4-20%) association of bone lesions in adult patients. [2] The sternum is a rare site of LCH involvement [3] and there has been no report of simultaneous involvement of lung and sternum in LCH. The patient, a 32-year-old male, presented with a 40-day history of anterior chest pain and swelling. US showed a low-echoic mass [Figure 1]a in the sternum with soft-tissue extension and cortical disruption, prompting the possibility of tuberculosis and metastasis. We noticed bilateral interstitial infiltration [Figure 1]b on the radiograph and the patient underwent HRCT. HRCT revealed bilateral diffuse infiltrates sparing the costophrenic angle, composed of well-defined small nodules with occasional cavitation [Figure 1]c. Under the strong impression of PLCH with concomitant sternal involvement, US-guided biopsy of the sternal lesion was done with no associated complications. The histologic findings were consistent with LCH [Figure 1]d, with immnohistochemistry revealing the following results: focal positive for S100; focal positive for CD3 in T cells; focal positive for L26 in B cells; negative for CD30 and CD15. Treatment with vinblastine and prednisone with mercaptopurine, brought a rapid symptom relief.

Although sternal involvement of LCH is rare and manifests with nonspecific physical and radiologic signs, PLCH presents with specific HRCT signs. Therefore, chest radiograph of a patient with a painful sternal mass should be scrutinized for any interstitial infiltrates that may lead to a specific imaging diagnosis, which was PLCH in this case.

To date, sternal LCH has been diagnosed using various surgical techniques. However, tissue diagnosis can be done percutaneously using US guidance as in this case, reducing the morbidity and the length of hospital stay.

References

1Vassallo R, Ryu JH, Schroeder DR, Decker PA, Limper AH. Clinical outcomes of pulmonary Langerhans'-cell histiocytosis in adults. N Engl J Med 2002;346:484-90.
2Sundar KM, Gosselin MV, Chung HL, Cahill BC. Pulmonary langerhans cell histiocytosis: Emerging concepts in pathobiology, radiology, and clinical evolution of disease. Chest 2003;123;1673-83.
3Tazi A. Adult pulmonary Langerhans' cell histiocytosis. Eur Respir J 2006;27:1272-85.