MRI for Diagnosis of Mycetoma or Madura Foot

magnetic resonance imaging for Diagnosis of Mycetoma or Madura Foot spatter in Circle sign a unique attri alonee of mycetoma infrastructure on MRI a deal of ii casesAggarwal A, Gupta M, Patel B N, Patel S BAbstractMycetoma or Madura Foot is a chronic localized granulomatous unhealthiness characterized by exuberant granulomatous create from raw stuff brass involving the subcutaneous plane. It is most common in tropical countries. Diagnosis has been traditionally done by microbiological culture and histopathological tissue diagnosing but these argon often difficult to obtain and frequently nonsensical. MRI has recently emerged as a promising technique for early and prompt diagnosis of Mycetoma with the definition of a highly specific sign called as besprinkle in Circle sign. We hereby present 2 cases showing this device characteristic Dot in isthmus sign on MRI and thereby establishing the diagnosis of Madura Foot.Patient 1A 52-year-old male farmer by stock presented with a painless inflation involving the left break up, which had been operated on elsewhere two times. Previous reports of surgery were not available. Examination revealed a non tender, large bump involving whole of the left foot and the ankle joint. It was associated with numerous chronic discharging sinuses. (Fig 1) superior general examination was unremarkable and the softening tissue was normal. Rotuine blood and biochemical investigations were withal unremarkable. athletic field radiograph revealed a soft tissue con mannikin in the left foot with advanced bony destruction mainly involving the tarsal, metatarsals and phalanges without each calcification. MRI scan was performed to evaluate the indisposition further. MRI showed a soft tissue rush lesion, diffuse hyper impregnation involving subcutaneous tissue, muscles, and intermuscular fascial planes. There were likewise manifold focal fluid collections seen in the fascial plane with ulceration of overlying skin. The muddle demonstrated characteristically conglomerate areas of double, inconspicuous, sensitive 34 mm oval to round hyperintense lesions, which were disconnected by a low-signal-intensity rim in the subcutaneous plane of the dorsum of the foot. The centre of few of these lesions showed a wee hypointense focus, resulting in the full point-in-circle sign (Figs. 2, 3). The underlying fig ups showed cortical erosions mainly involving the tarsal, metatarsals and phalanges. On the basis of the above clinical and radiological findings, a diagnosis of mycetoma foot was put forward. A biopsy was performed to confirm the diagnosis which revealed granulomatous inflammation and bearing of eumycetoma (Fig. 4).Patient 2A 37 year old male, complained of mass in the left foot for the past 2 years. Examination revealed septuple numerous discharging sinuses with skin ulcerations. The discharging sinuses did not contain any grains which is commonly pathognomonic of Madura mycosis. Plain frontal radiograph of the left foot shows soft tissue mass with severe destruction of the bone along with a palisade causa of periosteal reaction mainly involving the tarsals and metatarsals (Figs. 5). The persevering underwent MRI for evaluation and extent of the disease. Similarly, the lesion showed tag inflammatory changes in the left foot with cortical erosion, with micro-abscesses formation. The characteristic dot in circle sign (Figs. 6) was described and diagnosis of mycetoma foot was made. The patient underwent an excision biopsy. Histopathology showed eumycetoma.ImagesFigure 2. T2-weighted axial MR cut sectionsof the left foot shows all-inclusive inflammatorychanges. Multiple hyperintenselesions which were small and round in shape and separated by tissue of low signal intensityare noted. near of these lesions (arrows) show acentral small focus of hypointensity, resulting in the characteristicdot-in-circle sign.Figure 3 T2-weighted fat-saturated coronal MR hear ofthe left foo t shows manifold microabscesses separated bya low-intensity matrix seen posteriolaterally. Marked inflammatory changes with multiple fluid collections are noted in the fascial plane.Figure 4 Haematoxylin and Eosin( HE) fungous organismssurrounded by granulation tissue.Figure 6 T2-weighted axial MR imageof the left foot shows extensive inflammatorychanges with cortical erosion. Multiple small sphericalhyper-intense lesions separated by tissue of low signal intensityare noted. Some of these lesions show asmall foci of hypointensity centrally, resulting in thedot-in-circle sign. melodic line the presence of multiplemicroabscess.DiscussionMadurai Mycosis is a chronic granulomatous disease caused by 2 group of organisms, the Eumyces which are also called as true fungi or eumycetoma, and the Actinomyces, which are the filamentous form also called as Actinomycetales or actinomycetoma. The disease was first described in the Madurai district in the state of Tamil Nadu, hence the eponym Ma dura foot. The infective organisms are normal inhabitants of the soil and cause infection by direct implantation into the skin, most commonly the foot in individuals walking bare foot. Patients importantly present with multiple subcutaneous nodules which are characteristically painless. These may split up rise to fistulae formation, often associated with a purulent discharge. The disease progresses slowly and over long term leads to abscess formation, sinus tracts, osteomyelitis, and fistula formation ultimately resulting in severe deformity and disability if treatment is not provided 4 .Histologically the disease is characterized by formation of so called grains, which are found embedded in the abscesses. These grains are nothing but aggregates of the organism and are surrounded by extensive granulation tissue. Initially there is soft tissue lummox with induration which later progresses to form multiple discharging sinus with or without bone involvement. 5Radiological investig ations play a significant role in arriving at the diagnosis swiftly especially since tissue cultures are seldom diagnostic. Radiographs may be normal early in the disease process but later show varying degree of soft tissue swelling with destruction of the bone in form of sclerosis, cavity formation and classical palisade type of periosteal reaction. This is followed by expansion of the bone with scalloping of the cortex or osteoporosis. This physique mimics bacterial osteomyelitis but in mycetoma the bones are usually detsroyed from the outside, giving rise to characteristic Moth eaten appearance. 2The Dot in circle sign has emerged has a highly specific sign for the diagnosis of this condition and is based on the understanding of the pathogenesis of the disease process. It reflects the uniquepathological lark about of mycetoma and consists of multiple small round hyperintense lesions of size measuring around 3-5 mm surrounded by a hypointense rim. The small hyperintense lesions represent the granulation tissue and the surrounding hypointense rim represents the intervening stroma having fibrous septations. The low-signal intensity dot in the centre is due to the presence of fungal grains which causes a susceptibility payoff on MRI. This is a unique appearance and is easily recognisable in mycetoma. 1 This sign was proposed by Sarris et al. in 2003 on T2-weighted, STIR, and T1-weighted fat-saturated gadolinium enhanced images. goalWe conclude by saying that mycetoma is a severe debilitating disease with high unwholesomeness. Until now the diagnosis of the disease was limited to clinical see to it supplemented by biopsy and microbiological culture which were difficult to obtain and proved to be inconclusive in many cases. MRI has emerged as an excellent investigation in mycetoma and helps to arrive at the diagnosis much earlier in the course of disease thereby further helping in reducing the morbidity and rate of complications. Awareness of this characteri stic sign is important in bring in of the scarcity of reports that describe it in the literature and with increasing use of MRI in the evaluation of soft tissue tumours. 3RefS, Betty M, Manipadam MT, Cherian VM, Poonnoose PM, Oommen AT, et al. 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