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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_4532_Библиотеки_им_академика_М_И_Перельмана

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Normal and Abnormal Appearance of Nose and Paranasal Sinuses After Microendoscopic Surgery, Open Surg., and RT
Fig. 11.21. a Squamous cell carcinoma of left maxillary sinus. Remodeling of posterolateral wall is clearly shown on fat satu­rated T2 axial image (arrows). b Three years after treatment with radical maxillectomy, the TSE T2 axial image shows a regular double layer lining of the cavity: the internal one corresponding to the mucosa (arrows); the external one to the mature scar (arrowheads). Hypointensity is shown at the level of pterygoid process (PP) possibly consistent with sclerotic changes
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Fig. 11.22. Temporalis muscle fl ap. The pat ient had been treated
with right radical maxillectomy and left subtotal maxillectomy for an adenoid cystic carcinoma of right hard palate two years before. Adjuvant radiation therapy was delivered (56Gy). A free fl ap had to be removed for necrosis after irradiation. On TSE T2 coronal image the muscle is partially replaced by fat (white arrows).
elements: the aponeurosis and the striated pattern (Hud gins 2002). The aponeurosis, besides appear­ing denser on CT and more hypointense on MR in respect to the surrounding muscular bundles, in­dicates also the direction of the bulk of the muscle. The second element consists in the fan-shaped inner
structure of the muscle, which is clearly detectable on condition that more than a single MR plane is evalu­ated. Progressive atrophy of fl ap leads to replacement of muscular bundles by fat tissue signal.
During immediate to intermediate phase, edema and enhancement surrounding the fl ap are usually present. A variable reduction of both abnormalities is observed during the late phase. Characteristic fea­tures of myo-cutaneous fl aps are the presence of skin and subcutaneous fat, which show typical fi ndings on MR and CT.
A third category of post-operative changes encom­passes the modifi cations of the mucosal surface re­sulting from either subperiosteal dissection or from bone resection. Mucosal reactive changes and scar formation can be relevant, accounting for diffuse changes of the sinonasal tract mucosa, which can assume a polypoid confi guration due to increased thickening, and usually shows abnormal density and signal (Fig. 11.24). The resulting general pattern in­cludes a polypoid aspect of the mucosa lining the sinonasal cavities, with rim enhancement and low inner signal (density, intensity). Deviations from that pattern may be very diffi cult to separate from recurrent disease. Particularly, scar tissue may show imaging features at CT similar to mucosal thicken­ing. Early scar and granulation tissue usually have hyperintense signal on T2 and enhance after contrast agent administration (Loevner and Sonners 2002). Fibrosis is a hallmark of mature scar, it accounts for
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a
b
Fig. 11.23a,b. Temporalis muscle fl ap. a The patient had been
treated with left radical maxillectomy extended to infratem­poral fossa for an adenoid cystic carcinoma of the hard pal­ate. Three years after surgery, on the plain T1 axial image the muscle is clearly detected, its architecture well preserved (black arrows). Sclerotic changes of left pterygoid process are present (white arrows) b The patient was operated on with left radical maxillectomy, ethmoidectomy, orbital exenteration, the defect reconstructed with temporalis muscle, for a squamous cell carcinoma arising from maxillary sinus. Adjuvant radiation therapy was given (60Gy). Trismus developed about one month after irradiation. Follow up MR one year after surgery. On the post-contrast T1 axial image, the enhancing fatty muscle enters the cavity left by orbital exenteration running behind the scle­rotic frontal orbital process of frontal bone. The hypointense aponeurosis is well appreciated (black arrows). Asymmetric enlargement of cavernous sinus is seen after orbital exentera­tion (white arrows). The straight external outline does not sug- gest perineural spread (confi rmed on subsequent MR studies). Blockage of left sphenoid sinus is present (asterisk)
a more hypointense signal on T2 and a less tendency to enhance.
Synechiae can lead to stenosis of sinus drainage path­ways or blockage. Stenosis or occlusion of the lacrimal pathways account for the onset of epiphora. Dilation of the lacrimal sac should be noted and reported.
Post-operative bone changes are frequent, being related both to resection and to subperiosteal mu-
b
Fig. 11.24a,b. Follow of a patient treated for ethmoid inverted
papilloma with foci of squamous cell carcinoma nine years after surgery (same patient of fi gure 11.7). Post-contrast T1 in the axial plane. a Marked thickening of the mucosa lining the sinonasal cavities (arrows). b Incidental detection of a T1 undifferentiated carcinoma within left Rosenmüller fossa (ar- rows)
cosa dissection. On CT, sclerotic changes can be com­pounded to focal areas of bone dehiscence, or ero­sion. On MR, thickening of the cortical hypointense rim is observed, sometimes associated with focal more intense areas, and periosteal thickening. This can be detected on the masticator space surface of the posterolateral wall as a thin solid stripe lining the hypointense bone.
Normal and Abnormal Appearance of Nose and Paranasal Sinuses After Microendoscopic Surgery, Open Surg., and RT
11.4.4.2 Normal Post-radiation Therapy Imaging Changes
Since radiation therapy is seldom used as the ex­clusive treatment in malignant sinonasal tract neo­plasms, changes due to irradiation damage are in most patients added to those occurring after surgery. The pattern of the most frequent effects of radio­therapy on paranasal sinuses has been reported in patients treated for nasopharyngeal carcinoma, as part of the sinuses are routinely included within the irradiation portals (Chang et al. 2000). In these pa­tients, nasal symptoms - in the form of persistent na­sal obstruction, purulent discharge, posterior nasal dripping, and stuffy nose - are common.
Mucociliary damage by irradiation accounts for deterioration of the clearance function, which very often causes fl uid retention and mucosal thicken­ing. Pathologic fi ndings show squamous metapla­sia of the sinusal mucosa and thickening of the basement membrane, with disappearance of cilia. Fibrosis and thickening of the vessel walls within the stroma are also detected (Chang et al. 2000) (Fig. 11.25). In pre-irradiation disease-free sinuses, mucosal abnormalities are detected in up to 60% of patients on post treatment CT (Chang et al. 2000). Mucosal changes are similar to those observed af-
Fig. 11.25. Follow up after exclusive radiation therapy for a sphenoid sinus adenoid cystic carcinoma. The axial post­contrast T1 image is obtained four months after adjuvant of therapy. Subcutaneous and deep fat tissue (buccal fat pad, black asterisk) show a diffuse increase of reticulations indi­cating thickening. Reactive mucosal changes are seen in the maxillary sinuses (white asterisk in the left), asymmetric en­hancement is observed in the right medial pterygoid muscle (arrows)
ter surgery, they develop early, are reversible, last­ing for at least 4 years in about 50% of patients (Porter et al. 1996).
In our experience, patients operated on for ma­lignant neoplasm undergoing subsequent comple­tion radiotherapy develop less pronounced mucosal changes in the fi rst year from treatment. It may be that extensive subperiosteal dissection does not leave any mucosa, so that irradiation usually leads to de­velopment of a fi brotic lining of the treated sinonasal cavities. Only when mucosa regrows is reactive thick­ening usually observed.
Apart from changes in the sinonasal tract, irradia­tion effects modify the imaging fi ndings of adjacent tissues, particularly those located in the masticator space or in the nasopharynx.
Likewise mucosal abnormalities, the two most prominent masticator space tissues (fat, muscles) show dynamic changes which refl ect the acute and late effects of irradiation on tissues.
A few weeks after the completion of radiation treatment, infl ammatory changes and edema are prevalent, giving rise to diffuse heterogeneity of the MR signal of fat (which becomes denser at CT) and to thickening and diffuse enhancement of mastica­tor muscles. Bone marrow changes are also present
(hyperintensity on T2, hypointensity on plain T1, en­hancement).
Approximately 6 to 8 months after treatment, sub­acute infl ammatory modifi cations are replaced by the development of mature fi brosis, which is less vas­cularized. Masticator muscles progressively reduce in volume to normal size, while fatty changes may develop. The typical striation of muscular bundles provides reassurance that the muscle is “normal” (Fig. 11.26). While increased CT density of fat tissue persists, the hyperintensity observed on T2 reduces. Major salivary gland abnormalities include volume reduction and relevant enhancement on both CT and MR images (Becker et al. 1997; Nomayr et al. 2001).
Changes in the nasopharynx are characterized by reduction in size of the lymphoid tissue at the ad­enoid tonsil and along lateral recesses, variable thick­ening of the mucosa, and thickening of submucosal layers and fat planes surrounding the walls. A stiffer nasopharynx results, with hypointense (T2, plain T1) and non enhancing stripe of fat tissue surrounding its walls.
Within one year from radiation treatment, most imaging changes of masticator space, salivary glands
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and nasopharynx are stable, except for mucosal ab­normalities, which can still regress. Fatty replacement of bone marrow within the sphenoid bone, especially at the pterygoid process level, the clivus, and the ver­tebral bodies is a well known side effect of radiation treatment, which is related to the transformation of red into yellow bone marrow. Variable hyperintensity of bone marrow on plain T1 sequences may be seen.
Fig. 11.26. Post-radiation changes in both lateral pterygoid muscles (arrows) are characterized by non homogeneous en­hancement; the typical muscular striation is preserved
11.4.4.3 Imaging the Complications of Post-radiation Therapy
Apart from mucosal scars, which may sometimes lead to the formation of a mucocele (Rejab et al. 1991) (Fig. 11.27), the most common complications of ra­diation therapy include cranial neuropathies –optic neuritis being the most critical target, CNS radiation abnormalities, osteoradionecrosis – the mandible be­ing most frequently involved -, and development of radiation-associated tumors.
Optic neuritis secondary to irradiation and radia­tion retinopathy may present with progressive visual loss. This complication developed in up to 30% of a group of 78 patients treated by radiation therapy alone with curative intent (Katz et al. 2002). Although in most patients unilateral blindness was anticipated because of disease extent, in 5% of cases it developed unexpected due to optic neuropathy. On MR, thick­ening and enhancement of the involved nerve, optic tract or chiasm are observed (Fig. 11.28).
In case of ethmoid or sphenoid sinus neoplasms, radiation treatment portals do necessarily include a portion of CNS. Central nervous system involve- ment has been reported in less than 3% of patients treated for ethmoidal neoplasms (Gaucher et al.
2002). Nevertheless, its incidence is probably higher, as some patients may be asymptomatic and their le­sions go undetected. The time interval for the onset of symptoms ranges from a few weeks to several years.
ab
Fig. 11.27a-c. Frontal mucocele arising after radiation therapy for undifferentiated carcinoma of the right ethmoid. On TSE T2 coronal images, mucosal thickening involves both anterior naso-ethmoid cavities, thicker on the right side (arrowhead in a). a A frontal right frontal mucocele is demonstrated (arrows). b Diffuse changes of the cribriform plates, perpendicular lamina
(asterisk) and crista galli are seen. They are characterized by bone thickening and unsharp outlines, especially at the bone/CSF interface (arrows). Findings are related to previous invasion of the ethmoid by tumor. c On the axial plane remodeling of sinusal wall by the mucocele is shown (arrows)
c
Normal and Abnormal Appearance of Nose and Paranasal Sinuses After Microendoscopic Surgery, Open Surg., and RT
riod of radiation treatment itself, probably caused by damage to brain capillaries with rupture of the blood brain barrier and subsequent development of edema. Early-delayed changes occurs weeks to months after treatment, while late-delayed abnormalities appears months to years after therapy.
Early and early-delayed necrosis are character­ized by hyperintense T2 signal indicating edema and demyelination, which is often reversible. If the damage to the white matter progresses, radia­tion induced necrosis occurs. Late-delayed necrosis of the brain is generally irreversible, and some-
a
times fatal. Besides the presence of hyperintense T2 signals, which indicates demyelination foci in the white matter, imaging fi ndings include punctate, gyriform or serpiginous enhancement on post-con­trast T1, consistent with frank necrosis in the white matter (Gaucher et al. 2002). Mass effect, usually with variable enhancement at the periphery, is also noted (Rabin et al. 1996; Chong et al. 2000b, 2002). Sometimes, it may be diffi cult to differentiate radia­tion necrosis from recurrent intracranial ethmoidal or sphenoidal tumors with intracerebral invasion or from hematogenous metastases (Chong et al. 1997).
b
Careful analysis should permit to identify the pat­tern of a recurrent tumor, which is characterized by a mainly extradural location or epicenter and a minor intradural intracerebral component, from the exclusive intradural location of radiation necrosis (Chong et al. 2000b).
Radiation therapy can also induce in the brain mineralizing microangiopathy and telangiectasia (Va l k and Dillon 1991). Microangiopathy appears as multiple punctate calcifi cations in the cerebral cortex, brainstem, and basal ganglia. If deep perfo­rating arteries are involved, ischemia of the basal ganglia, thalamus, and deep white matter may occur.
c
Fig. 11.28a-c. Optic neuritis after radiation therapy, same pa-
tient of Figure 11.27. Severe, progressive vision impairment on left side. Post-contrast coronal T1 images show peripheral irregular enhancement of the intracranial portion of the left optic nerve (arrows in a and b). c No abnormality is seen at the level of the chiasm (arrows)
Telangiectasia, probably secondary to the develop­ment of collateral circulation, may lead to brain hem­orrhage (Gaensler et al. 1994).
Osteoradionecrosis of the mandible, though more often observed after treatment of oral carcinoma, may occur also after irradiation of sinonasal tract neoplasms, especially for maxillary sinus carcinoma. The imaging fi ndings are similar to bone necrosis in other areas. CT reveals the typical osseous fi ndings
Total dose, duration and fractionation infl uence the risk of developing such a complication. Depending on the interval from treatment, brain lesions due to irradiation are classifi ed into early, early-delayed and late-delayed. The deep white matter is typically involved with relative sparing of the cortex (Becker et al. 1997). Early lesions may develop during the pe-
of cortical disruption, trabecular disorganization, and fragmentation. Abnormal T1 hypointensity, T2 hyperintensity, and intense enhancement of the bone marrow in the involved mandible is usually shown on MR. Post-contrast fat saturated sequences can show the enhancing infl amed reaction surrounding the ne­crotic medullary bone (Fig. 11.29).
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Fig. 11.29a,b. Follow up after right radical maxillectomy and adjuvant radiation therapy for a squamous cell carcinoma three years after treatment. The patient complained of progressive trismus for 3 months. Coronal plain (a) and post-contrast (b) T1 images show increased thickness of right mandibular ramus. a A lesion arises from cancellous bone, destroys the cortical (white arrows), surrounded by remarkably sclerotic spongiosa and thickened cortical rim (arrowheads). Abnormal hypointense signal of the adjacent masseter muscle is seen (black arrows). Masticator space structures and fat signal are replaced by homogeneous hypointense signal (asterisk), which is associated with retraction of adjacent common nasal-oral cavity structure. Hard Palate (HP). b The osteonecrotic bone shows marked, heterogeneous enhancement. Infl ammatory changes of the adjacent masseter muscle give rise to mild enhancement (black arrow). The detectability of the muscular striation reassures about the non-neo­plastic nature. Non homogenous enhancement of the scar replacing masticator space structures is demonstrated (asterisk). Asymmetric enhancement of the right maxillary nerve (V2) compared to the opposite side, requires further studies to rule out perineural spread
R. Maroldi et al.
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In addition, abnormal diffuse enhancement in surrounding tissues and in the adjacent masseter and pterygoid muscles may be noted. Those muscles can be irregularly enlarged, appearing as space-occupy­ing lesions adjacent to the abnormal bone, mimick­ing recurrent disease. Abnormal T2 hyperintensity and relevant diffuse enhancement is usually present (Chong et al. 2000a).
Radiation-associated neoplasms of the head and neck occur in the radiation portal area, with a fre­quency ranging from 0.4 to 0.7% (Steeves and Bataini 1981; van der Laan et al. 1995) (Fig. 11.30). Other criteria for the diagnosis of a post-irradiation tumor include a histology different from that of the primary tumor and a latency period of at least 5 years (King et al. 2000).
A wide range of radiation-associated tumors has been reported, including sarcoma, meningioma, schwannoma, glioma, and squamous cell carcinoma (Rubinstein et al. 1989; Harrison et al. 1991; Mark et al. 1993). Osteosarcoma and malignant fi ­brous histiocytoma are the most frequent (Rabin et al. 1996).
11.4.4.4 Imaging of Local Recurrences
In the follow up, the radiologist may be faced with an asymptomatic recurrence or an already known relapse. In the fi rst case, which is the most challenging situation, knowledge of the most probable site of recurrence and of the imaging features of early recurrences is essential. A known local relapse raises different issues, specifi ­cally a careful assessment of its relationship with critical structures such as the orbit, the skull base, the brain, the cavernous sinus, and the internal carotid artery (Laccourreye et al. 1994; Lell et al. 2000).
In general, asymptomatic extra-mucosal recur­rences are more frequently expected close to the re­section area or at its boundary with fl aps.
Unlike primary tumors, abnormalities in symmetry (in comparison with the opposite side) due to treatment are so frequent to be commonly of limited usefulness. The resulting distorted anatomy is compounded of post treatment changes in residual structures, presence of a fl ap, and fi brous scar (Fig. 11.31-34). Therefore, the fi rst step in the interpretation of CT or MR consists in a careful identifi cation of the expected changes due
Normal and Abnormal Appearance of Nose and Paranasal Sinuses After Microendoscopic Surgery, Open Surg., and RT
Fig. 11.30a,b. Radiation-associated leiomyosarcoma eleven years after irradiation for nasopharyngeal undifferentiated carci­noma. On contrast enhanced coronal T1 image, the neoplasm arises from the masticator space muscles and invades the right sphenoid (white arrows on a and b). a Both the medial and lateral pterygoid muscles are invaded (black arrows). b The epicenter of tumor is located at the level of the foramen ovale. Although the mandibular nerve is thickened and shows slight enhance­ment (black arrows) only minor changes in the ipsilateral masticator muscles are noted. Invasion of the clivus is present (ar- rowheads)
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Fig. 11.31a,c. Follow up of left ethmoid rhabdomyosarcoma. TSE T2 images on coronal plane show the extent of tumor before
(a) two months (b) and four months after treatment (c). Progressive shrinkage of tumor (asterisk) leads to total disappearance of the lesion, leaving an abnormally remodeled middle turbinate (arrows in b and c)
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ba
Fig. 11.32a,b. Same patient of Figure 11.31. Nine months after the follow up study of Figure 11.31c, the onset of persisting head-
ache, leads the patient to an new study, which shows an extra-axial mass in the right frontal lobe (asterisk on a) corresponding to an epidural metastasis. Any recurrent lesion is seen in left ethmoid (arrows). b The post-contrast axial image shows the enhancing epidural nodule (black arrows), associated with adjacent linear enhancement which may suggest leptomeningeal metastasis (white arrows)
to previous therapy. Once expected changes and the corresponding structures (mucosa lining the sinuses, bony framework, fat, muscles, dura) are detected, any other abnormal signal should be carefully evaluated, especially focal masses. In case of previous surgery with/without adjuvant radiotherapy, the resulting fi ­brous scar should be distinguished from recurrent tu­mor; whereas in case of exclusive radiotherapy, is the tumor shrinkage with its transformation into imma­ture/mature scar to be differentiated from a relapse.
A combination of diagnostic strategies is gener­ally recommended. Since MR has a superior contrast resolution, it is commonly preferred to CT. If the ab­normal signal cannot be differentiated from fi brosis, a subsequent MR study may result defi nitive, other­wise a biopsy should be obtained.
However, MR imaging has been reported to be su­perior to CT only in differentiating recurrent tumor from mature fi brous scar, which has low signal inten­sity on all sequences and does not enhance (Gong et al. 1991; Lell et al. 2000). Immature fi brosis, viable tumor, tumor necrosis may all show homogenous to
Fig. 11.33. Same patient of Figure 11.31-32, subsequently treated with chemotherapy. The study obtained eight months after the one of Figure 11.32b does not show any recurrent
heterogeneous hyperintense signal on T2 (Chong and Fa n 1997; Lell et al. 2000). Nor can result de­cisive the pattern on post-contrast T1 sequences, as
Normal and Abnormal Appearance of Nose and Paranasal Sinuses After Microendoscopic Surgery, Open Surg., and RT
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a
Fig. 11.34a,b. Same patient of Figure 11.31-33, only one month after the MR examination of Figure 11.33. Diffuse leptomeningeal
metastasis is present (arrows)
the recurrent tumor can exhibit various degrees of contrast enhancement (Ng et al. 1999).
Dynamic contrast-enhanced MR imaging can po­tentially improve the diagnostic yield (Fig. 11.35). Data provided refl ects capillary blood fl ow, permeability, and the relative volume of extravascular extracellular space, resulting in quantitative parameters related to tumor angiogenesis (Tay lo r et al. 1999). Two quanti­tative parameters have been demonstrated to improve relapse detection in several areas of the body: the slope of enhancement over 60 seconds, which is related to tis­sue vascularization – i.e., the number of vessels, the de­gree of perfusion, and capillary permeability; and the maximum average enhancement which is dependent on the volume of the extracellular space (Moehler et al. 2001; Fischbein et al. 2003; Rahmouni et al. 2003). In the follow-up after surgery and/or radiotherapy of 27 head and neck and skull base tumors, we recently observed that the slope of enhancement and maxi­mum intensity averages of recurrences were signifi ­cantly steeper and higher, respectively, than in negative lesions (Piazzalunga et al. 2004).
The baseline MR examination remains a cor­nerstone reference for comparing areas with ab­normal signal to previous fi ndings (Fig. 11.36). MR
Fig. 11.35. Recurrent squamous cell carcinoma of left ethmoid after surgery (left radical maxillectomy with orbital exentera­tion), radiotherapy and chemotherapy. Color-coded image based on a pixel-by-pixel analysis of the slope of the enhance­ment curve. Yellow areas in the previous area of the pterygoid process (white arrows) indicate the relapse
b
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d
Fig. 11.36 a-f Multiple recurrences in a patient initially treated with craniofacial resection and adjuvant radiotherapy for an
ethmoid adenocarcinoma. Post-contrast T1 (a-d, f) and VIBE (e) images in the axial plane, obtained four months after the end of radiation treatment (a), seven months after previous image (b), four months after left medial maxillectomy (c), eight months after the previous study (d and e), four months after radical maxillectomy with myo-cutaneous and fascio-cutaneous fl aps (f). a The fi rst follow up study shows only marked infl ammatory reaction of the mucosa within the left maxillary sinus. b Submucosal recurrence is arising from left pterygopalatine fossa (arrows), with mucosal bulging. c The follow up after maxillectomy shows fi ndings consistent with post surgical changes, a smooth lining of the cavity is seen (arrows). d-e A second recurrent lesion develops from the interface between the maxillary sinus and the masticator space with extensive involvement of adjacent struc­tures (arrows). Both recurrent tumor and invasion of anterior maxillary sinus wall are more evident on VIBE image (e). f The temporalis myo-cutaneous fl ap (arrowheads) is clearly distinguished from the fascio-cutaneous (double arrowheads arrows) by means of its partially degenerated muscular architecture
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f