The existing optical microscopes form an image by collecting photons emitted from an object. Here we report on the experimental realization of microscopy without the need for direct optical communication with the sample. To achieve this, we have scanned a single gold nanoparticle acting as a nano-antenna in the near field of a sample and have studied the modification of its intrinsic radiative properties by monitoring its plasmon spectrum.PACS numbers: 07.79. Fc, 42.50.Lc, 78.67.Bf Over the years, several clever techniques such as darkfield, phase contrast, fluorescence, differential interference contrast, confocal, and scanning near-field microscopies have provided powerful ways of performing optical imaging. In all these methods, as in any other visual process, one "sees" an object when photons originating from it reach the detector. The details of the imaging mechanism depend sensitively on the intensity, phase and polarization of light both in the illumination and collection channels. The thought of recording optical images without receiving photons from the object, therefore, seems to be a contradiction in terms. In this Letter we show that this is indeed possible if one monitors the intrinsic spectral properties of a nanoscopic antenna scanned close to the sample.When an oscillating dipole is placed in confined geometries its radiative properties, such as eigenfrequency and linewidth, are modified [1,2]. In an intuitive picture these modifications are due to the interaction of the oscillating dipole with its image dipoles whereby the boundary materials and their distances to the oscillator determine the strength and phase of this interaction. In an alternative point of view the radiative changes are due to the modification of the density of photon states available for emission. In the context of recent developments in nano-optics, theoretical investigations have extended these concepts to subwavelength geometries and have shown that the linewidth [3,4,5,6,7] and the transition frequency [5,6] of a dipole also respond sensitively to the optical contrast of its nanoscopic environment.