Abstract

Fanconi anemia (FA) is a disease that could be accompanied by multiple abnormalities, such as growth retardation, bone marrow abnormalities, and cancer susceptibility. Among the FA patients, head and neck squamous cell cancer (HNSCC) is the most observed solid cancer. The life expectancy of patients with FA has increased with recent medical advances. Furthermore, HNSCC is diagnosed in 3% of FA patients, and half of these patients die because of their HNSCC. The median age of HNSCC patients with FA is 31, and according to the literature HNSCC incidence of FA, patients is more than 700-fold of the normal population. Here, we reported the treatment details and challenges we faced during hypopharyngeal cancer treatment in a FA patient.

Highlights

  • Fanconi anemia (FA) is a genetic bone marrow failure syndrome characterized by pancytopenia

  • FA patients are strongly prone to head and neck squamous cell cancer (HNSCC) development; they have an earlier onset for HNSCC [2]

  • In a study by Gluckman et al, five patients diagnosed with Fanconi anemia underwent hematopoietic stem cell transplantation after a preparation regimen with cyclophosphamide, and severe cyclophosphamide-related toxicity was observed in all of them

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Summary

Introduction

Fanconi anemia (FA) is a genetic bone marrow failure syndrome characterized by pancytopenia. To confirm the diagnosis of FA, we communicated with the related university hospital for the records of the patients 20 years ago They approved the diagnosis of FA with some peripheric blood sample studies without giving details. The patient's first notable characteristic was growth retardation manifested by short stature, microcephaly, and microphthalmia Afterward, she had swallowing difficulty for the last two years and had lost around 10 kg in the last six months. The remaining maintenance dosage was scheduled as 250 mg/m2 but could not be administered due to a sudden drop in blood count (white blood count to 0.48x103cells/uL) after four days of initial cetuximab and 10 days of RT Her treatment was terminated due to progressive cytopenia (Table 1), after receiving 21.2 Gy in 10 days for primary lesion.

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