Langerhans Cell Histiocytosis in a Five-Month-Old Infant

Clinical Image

Ann Hematol Oncol.2019; 6(3): 1237.

Langerhans Cell Histiocytosis in a Five-Month-Old Infant

Chi MH1¹, Cheng CD¹ and Yeh TC²*

¹Department of Pediatrics, Hsinchu Cathay General Hospital, Taiwan

²Division of Hematology & Oncology, Mackay Children’s Hospital, Taiwan

*Corresponding author: Yeh TC, Division of Hematology & Oncology, Mackay Children’s Hospital, 92 Sec. 2, Chung-San North Road, Taipei, Taiwan

Received: January 04, 2019; Accepted: February 11, 2019;Published: February 18, 2019

Keywords

Langerhans cell histiocytosis; Enlarged phalangeal bone; Granulation tissue

Clinical Image

A well-nourished 5-month-old boy presented with a 4-week history of swelling in his right middle finger. Physical examination did not find hepatosplenomegaly or lymphadenopathy, but an enlarged phalangeal bone (Figure 1). Laboratory examinations were within normal limits. X-ray examination revealed an isolated expansile lytic bone lesion without cortical destruction or periosteal reaction from metaphysis or diaphysis in the proximal phalanx of the right middle finger (Figure 2). Fine needle aspiration cytology was performed suggestive of an inflamed granulation tissue with atypical cells displaying irregular nuclei and ample cytoplasm. Immunohistochemical study of the atypical cells showed positive staining of CD1a, CD5, CD68 (KP1), Langerin, S-100 protein, and negative staining of CD20. The findings confirmed the diagnosis of Langerhans cell histiocytosis. The patient did not receive any treatment, but routine follow-up. One year later, the patient was asymptomatic and in good health.

Citation: Tufaro A, Garrisi VM, Kardhashi A, Gargano G, Liso DM, Atlante A, et al. Preliminary Report of Routine use of CA-125 and HE-4 in 26 Consecutive Patients Operated in a National Cancer Center. Ann Hematol Oncol. 2019; 6(2): 1232.