Nasopharyngeal inflammatory pseudotumor mimicking nasopharyngeal malignancy: a case report
Turki M. Bin Mahfoz
1790
ABSTRACTBackground: Inflammatory
pseudotumor (IPT) is a benign idiopathic inflammatory condition. Clinically, it
manifests as either a slow-growing tumor with little mass effect or
progressively destructive mass that resembles malignancy. Here, we present a
case of nasopharyngeal inflammatory pseudotumor mimicking nasopharyngeal
malignancy.
Case presentation: A
70-year-old male patient complained of mild right otalgia with decreased
hearing; there were no other otological symptoms or cranial nerve neuropathy.
Computed tomography (CT) revealed a suspicious soft tissue density in the right fossa of Rosenmüller
(pharyngeal recess), while magnetic
resonance imaging (MRI) identified a diffuse and homogeneous lesion in the
right fossa of Rosenmüller where
T1 and T2 images were enhanced and hypointense, respectively. The patient
underwent multiple right endonasal endoscopies for nasopharyngeal biopsy under
general anesthesia, which showed benign nasopharyngeal tissue with chronic
inflammatory cells and seromucous salivary inflammatory glands, without
evidence of carcinoma or lymphoma. Consequently, he was administered
corticosteroid therapy with good tolerability and response. There was no
clinical or radiological evidence of recurrence after a 1-year follow-up.
Conclusion: Diagnosis
of IPT is a challenge due to its malignancy-like characteristics. IPT
involving the nasopharynx has characteristic MRI findings, which, together with
clinical and laboratory presentations, help differentiate IPTs from malignant
tumors, especially nasopharyngeal carcinoma. However, to confirm
the diagnosis, a tissue biopsy is essential. Treatment of IPT
of the skull base is controversial and may involve corticosteroids, radiation
therapy, surgical excision, or multimodality depending on pathological subtype,
ease and safety of resection, the safety of high-dose corticosteroid use, the
surgeon's comfort, and the patient's preference. Other chemotherapeutic agents
with or without radiotherapy may be considered in steroid-resistant patients.
Keywords: Inflammatory pseudotumor,
magnetic resonance imaging, biopsy, corticosteroid, inflammatory
myofibroblastic tumor fossa of Rosenmüller, chronic inflammatory cells nasopharynx and skull base
Background: Inflammatory
pseudotumor (IPT) is a benign idiopathic inflammatory condition. Clinically, it
manifests as either a slow-growing tumor with little mass effect or
progressively destructive mass that resembles malignancy. Here, we present a
case of nasopharyngeal inflammatory pseudotumor mimicking nasopharyngeal
malignancy.
Case presentation: A
70-year-old male patient complained of mild right otalgia with decreased
hearing; there were no other otological symptoms or cranial nerve neuropathy.
Computed tomography (CT) revealed a suspicious soft tissue density in the right fossa of Rosenmüller
(pharyngeal recess), while magnetic
resonance imaging (MRI) identified a diffuse and homogeneous lesion in the
right fossa of Rosenmüller where
T1 and T2 images were enhanced and hypointense, respectively. The patient
underwent multiple right endonasal endoscopies for nasopharyngeal biopsy under
general anesthesia, which showed benign nasopharyngeal tissue with chronic
inflammatory cells and seromucous salivary inflammatory glands, without
evidence of carcinoma or lymphoma. Consequently, he was administered
corticosteroid therapy with good tolerability and response. There was no
clinical or radiological evidence of recurrence after a 1-year follow-up.
Conclusion: Diagnosis
of IPT is a challenge due to its malignancy-like characteristics. IPT
involving the nasopharynx has characteristic MRI findings, which, together with
clinical and laboratory presentations, help differentiate IPTs from malignant
tumors, especially nasopharyngeal carcinoma. However, to confirm
the diagnosis, a tissue biopsy is essential. Treatment of IPT
of the skull base is controversial and may involve corticosteroids, radiation
therapy, surgical excision, or multimodality depending on pathological subtype,
ease and safety of resection, the safety of high-dose corticosteroid use, the
surgeon's comfort, and the patient's preference. Other chemotherapeutic agents
with or without radiotherapy may be considered in steroid-resistant patients.
Keywords: Inflammatory pseudotumor,
magnetic resonance imaging, biopsy, corticosteroid, inflammatory
myofibroblastic tumor fossa of Rosenmüller, chronic inflammatory cells nasopharynx and skull base